Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.9763108_9769129del | CA915949116 | GRIN2A | c.2357-40_*41del c.1886-40_*247del n.1950-40_3686del c.1886-40_*41del c.2357-4181_*1806del c.1946-40_4025del n.1996-40_3732del c.1946-40_*247del c.2357-40_*247del c.2198-40_*41del c.2099-40_*41del c.2513-40_*41del c.2513-40_*247del | ClinVar |
16 | g.9764013C>A | CA277537103 | GRIN2A | c.3531G>T (p.Gly1177=) c.3060G>T (p.Gly1020=) n.3124G>T c.*901G>T (n.*901G>T) c.3120G>T (p.Gly1040=) n.3170G>T c.3372G>T (p.Gly1124=) c.3273G>T (p.Gly1091=) c.3687G>T (p.Gly1229=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.9764013C= | CA2206693010 | GRIN2A | c.3531G= (p.Gly1177=) c.3060G= (p.Gly1020=) n.3124G= c.*901G= (n.*901G=) c.3120G= (p.Gly1040=) n.3170G= c.3372G= (p.Gly1124=) c.3273G= (p.Gly1091=) c.3687G= (p.Gly1229=) | |
16 | g.9764013C>G | CA493693301 | GRIN2A | c.3531G>C (p.Gly1177=) c.3060G>C (p.Gly1020=) n.3124G>C c.*901G>C (n.*901G>C) c.3120G>C (p.Gly1040=) n.3170G>C c.3372G>C (p.Gly1124=) c.3273G>C (p.Gly1091=) c.3687G>C (p.Gly1229=) | dbSNP |
16 | g.9764013C>T | CA493693302 | GRIN2A | c.3531G>A (p.Gly1177=) c.3060G>A (p.Gly1020=) n.3124G>A c.*901G>A (n.*901G>A) c.3120G>A (p.Gly1040=) n.3170G>A c.3372G>A (p.Gly1124=) c.3273G>A (p.Gly1091=) c.3687G>A (p.Gly1229=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
16 | g.9764014C>A | CA394707419 | GRIN2A | c.3530G>T (p.Gly1177Val) c.3059G>T (p.Gly1020Val) n.3123G>T c.*900G>T (n.*900G>T) c.3119G>T (p.Gly1040Val) n.3169G>T c.3371G>T (p.Gly1124Val) c.3272G>T (p.Gly1091Val) c.3686G>T (p.Gly1229Val) | |
16 | g.9764014C= | CA2206693011 | GRIN2A | c.3530G= (p.Gly1177=) c.3059G= (p.Gly1020=) n.3123G= c.*900G= (n.*900G=) c.3119G= (p.Gly1040=) n.3169G= c.3371G= (p.Gly1124=) c.3272G= (p.Gly1091=) c.3686G= (p.Gly1229=) | |
16 | g.9764014C>G | CA394707420 | GRIN2A | c.3530G>C (p.Gly1177Ala) c.3059G>C (p.Gly1020Ala) n.3123G>C c.*900G>C (n.*900G>C) c.3119G>C (p.Gly1040Ala) n.3169G>C c.3371G>C (p.Gly1124Ala) c.3272G>C (p.Gly1091Ala) c.3686G>C (p.Gly1229Ala) | dbSNP |
16 | g.9764014C>T | CA7896297 | GRIN2A | c.3530G>A (p.Gly1177Glu) c.3059G>A (p.Gly1020Glu) n.3123G>A c.*900G>A (n.*900G>A) c.3119G>A (p.Gly1040Glu) n.3169G>A c.3371G>A (p.Gly1124Glu) c.3272G>A (p.Gly1091Glu) c.3686G>A (p.Gly1229Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.9764015C>A | CA394707421 | GRIN2A | c.3529G>T (p.Gly1177Trp) c.3058G>T (p.Gly1020Trp) n.3122G>T c.*899G>T (n.*899G>T) c.3118G>T (p.Gly1040Trp) n.3168G>T c.3370G>T (p.Gly1124Trp) c.3271G>T (p.Gly1091Trp) c.3685G>T (p.Gly1229Trp) | |
16 | g.9764015C>G | CA394707422 | GRIN2A | c.3529G>C (p.Gly1177Arg) c.3058G>C (p.Gly1020Arg) n.3122G>C c.*899G>C (n.*899G>C) c.3118G>C (p.Gly1040Arg) n.3168G>C c.3370G>C (p.Gly1124Arg) c.3271G>C (p.Gly1091Arg) c.3685G>C (p.Gly1229Arg) | dbSNP |
16 | g.9764015C>T | CA394707423 | GRIN2A | c.3529G>A (p.Gly1177Arg) c.3058G>A (p.Gly1020Arg) n.3122G>A c.*899G>A (n.*899G>A) c.3118G>A (p.Gly1040Arg) n.3168G>A c.3370G>A (p.Gly1124Arg) c.3271G>A (p.Gly1091Arg) c.3685G>A (p.Gly1229Arg) | COSMIC |
16 | g.9764016C>A | CA394707424 | GRIN2A | c.3528G>T (p.Glu1176Asp) c.3057G>T (p.Glu1019Asp) n.3121G>T c.*898G>T (n.*898G>T) c.3117G>T (p.Glu1039Asp) n.3167G>T c.3369G>T (p.Glu1123Asp) c.3270G>T (p.Glu1090Asp) c.3684G>T (p.Glu1228Asp) | dbSNP |
16 | g.9764016C>G | CA394707425 | GRIN2A | c.3528G>C (p.Glu1176Asp) c.3057G>C (p.Glu1019Asp) n.3121G>C c.*898G>C (n.*898G>C) c.3117G>C (p.Glu1039Asp) n.3167G>C c.3369G>C (p.Glu1123Asp) c.3270G>C (p.Glu1090Asp) c.3684G>C (p.Glu1228Asp) | |
16 | g.9764016C>T | CA493693312 | GRIN2A | c.3528G>A (p.Glu1176=) c.3057G>A (p.Glu1019=) n.3121G>A c.*898G>A (n.*898G>A) c.3117G>A (p.Glu1039=) n.3167G>A c.3369G>A (p.Glu1123=) c.3270G>A (p.Glu1090=) c.3684G>A (p.Glu1228=) | dbSNP gnomAD v4 |
16 | g.9764017T>A | CA394707426 | GRIN2A | c.3527A>T (p.Glu1176Val) c.3056A>T (p.Glu1019Val) n.3120A>T c.*897A>T (n.*897A>T) c.3116A>T (p.Glu1039Val) n.3166A>T c.3368A>T (p.Glu1123Val) c.3269A>T (p.Glu1090Val) c.3683A>T (p.Glu1228Val) | dbSNP |
16 | g.9764017T>C | CA394707427 | GRIN2A | c.3527A>G (p.Glu1176Gly) c.3056A>G (p.Glu1019Gly) n.3120A>G c.*897A>G (n.*897A>G) c.3116A>G (p.Glu1039Gly) n.3166A>G c.3368A>G (p.Glu1123Gly) c.3269A>G (p.Glu1090Gly) c.3683A>G (p.Glu1228Gly) | dbSNP |
16 | g.9764017T>G | CA394707428 | GRIN2A | c.3527A>C (p.Glu1176Ala) c.3056A>C (p.Glu1019Ala) n.3120A>C c.*897A>C (n.*897A>C) c.3116A>C (p.Glu1039Ala) n.3166A>C c.3368A>C (p.Glu1123Ala) c.3269A>C (p.Glu1090Ala) c.3683A>C (p.Glu1228Ala) | |
16 | g.9764018C>A | CA394707429 | GRIN2A | c.3526G>T (p.Glu1176Ter) c.3055G>T (p.Glu1019Ter) n.3119G>T c.*896G>T (n.*896G>T) c.3115G>T (p.Glu1039Ter) n.3165G>T c.3367G>T (p.Glu1123Ter) c.3268G>T (p.Glu1090Ter) c.3682G>T (p.Glu1228Ter) | dbSNP COSMIC |
16 | g.9764018C= | CA2206693012 | GRIN2A | c.3526G= (p.Glu1176=) c.3055G= (p.Glu1019=) n.3119G= c.*896G= (n.*896G=) c.3115G= (p.Glu1039=) n.3165G= c.3367G= (p.Glu1123=) c.3268G= (p.Glu1090=) c.3682G= (p.Glu1228=) | |
16 | g.9764018C>G | CA394707430 | GRIN2A | c.3526G>C (p.Glu1176Gln) c.3055G>C (p.Glu1019Gln) n.3119G>C c.*896G>C (n.*896G>C) c.3115G>C (p.Glu1039Gln) n.3165G>C c.3367G>C (p.Glu1123Gln) c.3268G>C (p.Glu1090Gln) c.3682G>C (p.Glu1228Gln) | ClinVar dbSNP gnomAD v4 |
16 | g.9764018C>T | CA394707431 | GRIN2A | c.3526G>A (p.Glu1176Lys) c.3055G>A (p.Glu1019Lys) n.3119G>A c.*896G>A (n.*896G>A) c.3115G>A (p.Glu1039Lys) n.3165G>A c.3367G>A (p.Glu1123Lys) c.3268G>A (p.Glu1090Lys) c.3682G>A (p.Glu1228Lys) | dbSNP gnomAD v4 |
16 | g.9764019T>A | CA394707432 | GRIN2A | c.3525A>T (p.Glu1175Asp) c.3054A>T (p.Glu1018Asp) n.3118A>T c.*895A>T (n.*895A>T) c.3114A>T (p.Glu1038Asp) n.3164A>T c.3366A>T (p.Glu1122Asp) c.3267A>T (p.Glu1089Asp) c.3681A>T (p.Glu1227Asp) | ClinVar dbSNP |
16 | g.9764019T>C | CA493693327 | GRIN2A | c.3525A>G (p.Glu1175=) c.3054A>G (p.Glu1018=) n.3118A>G c.*895A>G (n.*895A>G) c.3114A>G (p.Glu1038=) n.3164A>G c.3366A>G (p.Glu1122=) c.3267A>G (p.Glu1089=) c.3681A>G (p.Glu1227=) | dbSNP |
16 | g.9764019T>G | CA394707433 | GRIN2A | c.3525A>C (p.Glu1175Asp) c.3054A>C (p.Glu1018Asp) n.3118A>C c.*895A>C (n.*895A>C) c.3114A>C (p.Glu1038Asp) n.3164A>C c.3366A>C (p.Glu1122Asp) c.3267A>C (p.Glu1089Asp) c.3681A>C (p.Glu1227Asp) | |
16 | g.9764019T= | CA2206693013 | GRIN2A | c.3525A= (p.Glu1175=) c.3054A= (p.Glu1018=) n.3118A= c.*895A= (n.*895A=) c.3114A= (p.Glu1038=) n.3164A= c.3366A= (p.Glu1122=) c.3267A= (p.Glu1089=) c.3681A= (p.Glu1227=) | |
16 | g.9764020T>A | CA394707434 | GRIN2A | c.3524A>T (p.Glu1175Val) c.3053A>T (p.Glu1018Val) n.3117A>T c.*894A>T (n.*894A>T) c.3113A>T (p.Glu1038Val) n.3163A>T c.3365A>T (p.Glu1122Val) c.3266A>T (p.Glu1089Val) c.3680A>T (p.Glu1227Val) | dbSNP |
16 | g.9764020T>C | CA394707435 | GRIN2A | c.3524A>G (p.Glu1175Gly) c.3053A>G (p.Glu1018Gly) n.3117A>G c.*894A>G (n.*894A>G) c.3113A>G (p.Glu1038Gly) n.3163A>G c.3365A>G (p.Glu1122Gly) c.3266A>G (p.Glu1089Gly) c.3680A>G (p.Glu1227Gly) | |
16 | g.9764020T>G | CA394707436 | GRIN2A | c.3524A>C (p.Glu1175Ala) c.3053A>C (p.Glu1018Ala) n.3117A>C c.*894A>C (n.*894A>C) c.3113A>C (p.Glu1038Ala) n.3163A>C c.3365A>C (p.Glu1122Ala) c.3266A>C (p.Glu1089Ala) c.3680A>C (p.Glu1227Ala) | |
16 | g.9764021C>A | CA394707438 | GRIN2A | c.3523G>T (p.Glu1175Ter) c.3052G>T (p.Glu1018Ter) n.3116G>T c.*893G>T (n.*893G>T) c.3112G>T (p.Glu1038Ter) n.3162G>T c.3364G>T (p.Glu1122Ter) c.3265G>T (p.Glu1089Ter) c.3679G>T (p.Glu1227Ter) | dbSNP |
16 | g.9764021C= | CA2206693014 | GRIN2A | c.3523G= (p.Glu1175=) c.3052G= (p.Glu1018=) n.3116G= c.*893G= (n.*893G=) c.3112G= (p.Glu1038=) n.3162G= c.3364G= (p.Glu1122=) c.3265G= (p.Glu1089=) c.3679G= (p.Glu1227=) | |
16 | g.9764021C>G | CA394707437 | GRIN2A | c.3523G>C (p.Glu1175Gln) c.3052G>C (p.Glu1018Gln) n.3116G>C c.*893G>C (n.*893G>C) c.3112G>C (p.Glu1038Gln) n.3162G>C c.3364G>C (p.Glu1122Gln) c.3265G>C (p.Glu1089Gln) c.3679G>C (p.Glu1227Gln) | dbSNP |
16 | g.9764021C>T | CA277537117 | GRIN2A | c.3523G>A (p.Glu1175Lys) c.3052G>A (p.Glu1018Lys) n.3116G>A c.*893G>A (n.*893G>A) c.3112G>A (p.Glu1038Lys) n.3162G>A c.3364G>A (p.Glu1122Lys) c.3265G>A (p.Glu1089Lys) c.3679G>A (p.Glu1227Lys) | dbSNP COSMIC |
16 | g.9764022A= | CA2206693015 | GRIN2A | c.3522T= (p.Asn1174=) c.3051T= (p.Asn1017=) n.3115T= c.*892T= (n.*892T=) c.3111T= (p.Asn1037=) n.3161T= c.3363T= (p.Asn1121=) c.3264T= (p.Asn1088=) c.3678T= (p.Asn1226=) | |
16 | g.9764022A>C | CA394707439 | GRIN2A | c.3522T>G (p.Asn1174Lys) c.3051T>G (p.Asn1017Lys) n.3115T>G c.*892T>G (n.*892T>G) c.3111T>G (p.Asn1037Lys) n.3161T>G c.3363T>G (p.Asn1121Lys) c.3264T>G (p.Asn1088Lys) c.3678T>G (p.Asn1226Lys) | |
16 | g.9764022A>G | CA7896298 | GRIN2A | c.3522T>C (p.Asn1174=) c.3051T>C (p.Asn1017=) n.3115T>C c.*892T>C (n.*892T>C) c.3111T>C (p.Asn1037=) n.3161T>C c.3363T>C (p.Asn1121=) c.3264T>C (p.Asn1088=) c.3678T>C (p.Asn1226=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.9764022A>T | CA7896299 | GRIN2A | c.3522T>A (p.Asn1174Lys) c.3051T>A (p.Asn1017Lys) n.3115T>A c.*892T>A (n.*892T>A) c.3111T>A (p.Asn1037Lys) n.3161T>A c.3363T>A (p.Asn1121Lys) c.3264T>A (p.Asn1088Lys) c.3678T>A (p.Asn1226Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.9764023T>A | CA394707440 | GRIN2A | c.3521A>T (p.Asn1174Ile) c.3050A>T (p.Asn1017Ile) n.3114A>T c.*891A>T (n.*891A>T) c.3110A>T (p.Asn1037Ile) n.3160A>T c.3362A>T (p.Asn1121Ile) c.3263A>T (p.Asn1088Ile) c.3677A>T (p.Asn1226Ile) | dbSNP |
16 | g.9764023T>C | CA394707441 | GRIN2A | c.3521A>G (p.Asn1174Ser) c.3050A>G (p.Asn1017Ser) n.3114A>G c.*891A>G (n.*891A>G) c.3110A>G (p.Asn1037Ser) n.3160A>G c.3362A>G (p.Asn1121Ser) c.3263A>G (p.Asn1088Ser) c.3677A>G (p.Asn1226Ser) | |
16 | g.9764023T>G | CA394707442 | GRIN2A | c.3521A>C (p.Asn1174Thr) c.3050A>C (p.Asn1017Thr) n.3114A>C c.*891A>C (n.*891A>C) c.3110A>C (p.Asn1037Thr) n.3160A>C c.3362A>C (p.Asn1121Thr) c.3263A>C (p.Asn1088Thr) c.3677A>C (p.Asn1226Thr) | |
16 | g.9764024T>A | CA394707443 | GRIN2A | c.3520A>T (p.Asn1174Tyr) c.3049A>T (p.Asn1017Tyr) n.3113A>T c.*890A>T (n.*890A>T) c.3109A>T (p.Asn1037Tyr) n.3159A>T c.3361A>T (p.Asn1121Tyr) c.3262A>T (p.Asn1088Tyr) c.3676A>T (p.Asn1226Tyr) | dbSNP |
16 | g.9764024T>C | CA394707444 | GRIN2A | c.3520A>G (p.Asn1174Asp) c.3049A>G (p.Asn1017Asp) n.3113A>G c.*890A>G (n.*890A>G) c.3109A>G (p.Asn1037Asp) n.3159A>G c.3361A>G (p.Asn1121Asp) c.3262A>G (p.Asn1088Asp) c.3676A>G (p.Asn1226Asp) | dbSNP gnomAD v4 |
16 | g.9764024T>G | CA394707445 | GRIN2A | c.3520A>C (p.Asn1174His) c.3049A>C (p.Asn1017His) n.3113A>C c.*890A>C (n.*890A>C) c.3109A>C (p.Asn1037His) n.3159A>C c.3361A>C (p.Asn1121His) c.3262A>C (p.Asn1088His) c.3676A>C (p.Asn1226His) | |
16 | g.9764025A= | CA2206693016 | GRIN2A | c.3519T= (p.His1173=) c.3048T= (p.His1016=) n.3112T= c.*889T= (n.*889T=) c.3108T= (p.His1036=) n.3158T= c.3360T= (p.His1120=) c.3261T= (p.His1087=) c.3675T= (p.His1225=) | |
16 | g.9764025A>C | CA394707446 | GRIN2A | c.3519T>G (p.His1173Gln) c.3048T>G (p.His1016Gln) n.3112T>G c.*889T>G (n.*889T>G) c.3108T>G (p.His1036Gln) n.3158T>G c.3360T>G (p.His1120Gln) c.3261T>G (p.His1087Gln) c.3675T>G (p.His1225Gln) | |
16 | g.9764025A>G | CA493693336 | GRIN2A | c.3519T>C (p.His1173=) c.3048T>C (p.His1016=) n.3112T>C c.*889T>C (n.*889T>C) c.3108T>C (p.His1036=) n.3158T>C c.3360T>C (p.His1120=) c.3261T>C (p.His1087=) c.3675T>C (p.His1225=) | |
16 | g.9764025A>T | CA394707447 | GRIN2A | c.3519T>A (p.His1173Gln) c.3048T>A (p.His1016Gln) n.3112T>A c.*889T>A (n.*889T>A) c.3108T>A (p.His1036Gln) n.3158T>A c.3360T>A (p.His1120Gln) c.3261T>A (p.His1087Gln) c.3675T>A (p.His1225Gln) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.9764026T>A | CA394707448 | GRIN2A | c.3518A>T (p.His1173Leu) c.3047A>T (p.His1016Leu) n.3111A>T c.*888A>T (n.*888A>T) c.3107A>T (p.His1036Leu) n.3157A>T c.3359A>T (p.His1120Leu) c.3260A>T (p.His1087Leu) c.3674A>T (p.His1225Leu) | dbSNP |
16 | g.9764026T>C | CA277537159 | GRIN2A | c.3518A>G (p.His1173Arg) c.3047A>G (p.His1016Arg) n.3111A>G c.*888A>G (n.*888A>G) c.3107A>G (p.His1036Arg) n.3157A>G c.3359A>G (p.His1120Arg) c.3260A>G (p.His1087Arg) c.3674A>G (p.His1225Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.9764026T>G | CA394707449 | GRIN2A | c.3518A>C (p.His1173Pro) c.3047A>C (p.His1016Pro) n.3111A>C c.*888A>C (n.*888A>C) c.3107A>C (p.His1036Pro) n.3157A>C c.3359A>C (p.His1120Pro) c.3260A>C (p.His1087Pro) c.3674A>C (p.His1225Pro) | dbSNP |
16 | g.9764026T= | CA2206693017 | GRIN2A | c.3518A= (p.His1173=) c.3047A= (p.His1016=) n.3111A= c.*888A= (n.*888A=) c.3107A= (p.His1036=) n.3157A= c.3359A= (p.His1120=) c.3260A= (p.His1087=) c.3674A= (p.His1225=) | |
16 | g.9764027G>A | CA394707452 | GRIN2A | c.3517C>T (p.His1173Tyr) c.3046C>T (p.His1016Tyr) n.3110C>T c.*887C>T (n.*887C>T) c.3106C>T (p.His1036Tyr) n.3156C>T c.3358C>T (p.His1120Tyr) c.3259C>T (p.His1087Tyr) c.3673C>T (p.His1225Tyr) | dbSNP |
16 | g.9764027G>C | CA394707451 | GRIN2A | c.3517C>G (p.His1173Asp) c.3046C>G (p.His1016Asp) n.3110C>G c.*887C>G (n.*887C>G) c.3106C>G (p.His1036Asp) n.3156C>G c.3358C>G (p.His1120Asp) c.3259C>G (p.His1087Asp) c.3673C>G (p.His1225Asp) | dbSNP gnomAD v4 |
16 | g.9764027G>T | CA394707450 | GRIN2A | c.3517C>A (p.His1173Asn) c.3046C>A (p.His1016Asn) n.3110C>A c.*887C>A (n.*887C>A) c.3106C>A (p.His1036Asn) n.3156C>A c.3358C>A (p.His1120Asn) c.3259C>A (p.His1087Asn) c.3673C>A (p.His1225Asn) | |
16 | g.9764028C>A | CA7896300 | GRIN2A | c.3516G>T (p.Leu1172Phe) c.3045G>T (p.Leu1015Phe) n.3109G>T c.*886G>T (n.*886G>T) c.3105G>T (p.Leu1035Phe) n.3155G>T c.3357G>T (p.Leu1119Phe) c.3258G>T (p.Leu1086Phe) c.3672G>T (p.Leu1224Phe) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.9764028C= | CA2206693018 | GRIN2A | c.3516G= (p.Leu1172=) c.3045G= (p.Leu1015=) n.3109G= c.*886G= (n.*886G=) c.3105G= (p.Leu1035=) n.3155G= c.3357G= (p.Leu1119=) c.3258G= (p.Leu1086=) c.3672G= (p.Leu1224=) | |
16 | g.9764028C>G | CA394707453 | GRIN2A | c.3516G>C (p.Leu1172Phe) c.3045G>C (p.Leu1015Phe) n.3109G>C c.*886G>C (n.*886G>C) c.3105G>C (p.Leu1035Phe) n.3155G>C c.3357G>C (p.Leu1119Phe) c.3258G>C (p.Leu1086Phe) c.3672G>C (p.Leu1224Phe) | dbSNP |
16 | g.9764028C>T | CA493693348 | GRIN2A | c.3516G>A (p.Leu1172=) c.3045G>A (p.Leu1015=) n.3109G>A c.*886G>A (n.*886G>A) c.3105G>A (p.Leu1035=) n.3155G>A c.3357G>A (p.Leu1119=) c.3258G>A (p.Leu1086=) c.3672G>A (p.Leu1224=) | dbSNP |
16 | g.9764029A= | CA2206693019 | GRIN2A | c.3515T= (p.Leu1172=) c.3044T= (p.Leu1015=) n.3108T= c.*885T= (n.*885T=) c.3104T= (p.Leu1035=) n.3154T= c.3356T= (p.Leu1119=) c.3257T= (p.Leu1086=) c.3671T= (p.Leu1224=) | |
16 | g.9764029A>C | CA394707454 | GRIN2A | c.3515T>G (p.Leu1172Trp) c.3044T>G (p.Leu1015Trp) n.3108T>G c.*885T>G (n.*885T>G) c.3104T>G (p.Leu1035Trp) n.3154T>G c.3356T>G (p.Leu1119Trp) c.3257T>G (p.Leu1086Trp) c.3671T>G (p.Leu1224Trp) | |
16 | g.9764029A>G | CA394707455 | GRIN2A | c.3515T>C (p.Leu1172Ser) c.3044T>C (p.Leu1015Ser) n.3108T>C c.*885T>C (n.*885T>C) c.3104T>C (p.Leu1035Ser) n.3154T>C c.3356T>C (p.Leu1119Ser) c.3257T>C (p.Leu1086Ser) c.3671T>C (p.Leu1224Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
16 | g.9764029A>T | CA394707456 | GRIN2A | c.3515T>A (p.Leu1172Ter) c.3044T>A (p.Leu1015Ter) n.3108T>A c.*885T>A (n.*885T>A) c.3104T>A (p.Leu1035Ter) n.3154T>A c.3356T>A (p.Leu1119Ter) c.3257T>A (p.Leu1086Ter) c.3671T>A (p.Leu1224Ter) | dbSNP |
16 | g.9764030A>C | CA394707457 | GRIN2A | c.3514T>G (p.Leu1172Val) c.3043T>G (p.Leu1015Val) n.3107T>G c.*884T>G (n.*884T>G) c.3103T>G (p.Leu1035Val) n.3153T>G c.3355T>G (p.Leu1119Val) c.3256T>G (p.Leu1086Val) c.3670T>G (p.Leu1224Val) | |
16 | g.9764030A>G | CA493693356 | GRIN2A | c.3514T>C (p.Leu1172=) c.3043T>C (p.Leu1015=) n.3107T>C c.*884T>C (n.*884T>C) c.3103T>C (p.Leu1035=) n.3153T>C c.3355T>C (p.Leu1119=) c.3256T>C (p.Leu1086=) c.3670T>C (p.Leu1224=) | gnomAD v4 |
16 | g.9764030A>T | CA394707458 | GRIN2A | c.3514T>A (p.Leu1172Met) c.3043T>A (p.Leu1015Met) n.3107T>A c.*884T>A (n.*884T>A) c.3103T>A (p.Leu1035Met) n.3153T>A c.3355T>A (p.Leu1119Met) c.3256T>A (p.Leu1086Met) c.3670T>A (p.Leu1224Met) | |
16 | g.9764030_9764031del | CA2508563121 | GRIN2A | c.3513_3514del (p.Leu1172AlafsTer2) c.3042_3043del (p.Leu1015AlafsTer2) n.3106_3107del c.*883_*884del (n.*883_*884del) c.3102_3103del (p.Leu1035AlafsTer2) n.3152_3153del c.3354_3355del (p.Leu1119AlafsTer2) c.3255_3256del (p.Leu1086AlafsTer2) c.3669_3670del (p.Leu1224AlafsTer2) | |
16 | g.9764031G>A | CA493693360 | GRIN2A | c.3513C>T (p.Pro1171=) c.3042C>T (p.Pro1014=) n.3106C>T c.*883C>T (n.*883C>T) c.3102C>T (p.Pro1034=) n.3152C>T c.3354C>T (p.Pro1118=) c.3255C>T (p.Pro1085=) c.3669C>T (p.Pro1223=) | ClinVar dbSNP gnomAD v4 |
16 | g.9764031G>C | CA493693362 | GRIN2A | c.3513C>G (p.Pro1171=) c.3042C>G (p.Pro1014=) n.3106C>G c.*883C>G (n.*883C>G) c.3102C>G (p.Pro1034=) n.3152C>G c.3354C>G (p.Pro1118=) c.3255C>G (p.Pro1085=) c.3669C>G (p.Pro1223=) | dbSNP |
16 | g.9764031G= | CA2206693020 | GRIN2A | c.3513C= (p.Pro1171=) c.3042C= (p.Pro1014=) n.3106C= c.*883C= (n.*883C=) c.3102C= (p.Pro1034=) n.3152C= c.3354C= (p.Pro1118=) c.3255C= (p.Pro1085=) c.3669C= (p.Pro1223=) | |
16 | g.9764031G>T | CA493693361 | GRIN2A | c.3513C>A (p.Pro1171=) c.3042C>A (p.Pro1014=) n.3106C>A c.*883C>A (n.*883C>A) c.3102C>A (p.Pro1034=) n.3152C>A c.3354C>A (p.Pro1118=) c.3255C>A (p.Pro1085=) c.3669C>A (p.Pro1223=) | dbSNP |
16 | g.9764032G>A | CA394707459 | GRIN2A | c.3512C>T (p.Pro1171Leu) c.3041C>T (p.Pro1014Leu) n.3105C>T c.*882C>T (n.*882C>T) c.3101C>T (p.Pro1034Leu) n.3151C>T c.3353C>T (p.Pro1118Leu) c.3254C>T (p.Pro1085Leu) c.3668C>T (p.Pro1223Leu) | COSMIC |
16 | g.9764032G>C | CA394707460 | GRIN2A | c.3512C>G (p.Pro1171Arg) c.3041C>G (p.Pro1014Arg) n.3105C>G c.*882C>G (n.*882C>G) c.3101C>G (p.Pro1034Arg) n.3151C>G c.3353C>G (p.Pro1118Arg) c.3254C>G (p.Pro1085Arg) c.3668C>G (p.Pro1223Arg) | |
16 | g.9764032G>T | CA394707461 | GRIN2A | c.3512C>A (p.Pro1171His) c.3041C>A (p.Pro1014His) n.3105C>A c.*882C>A (n.*882C>A) c.3101C>A (p.Pro1034His) n.3151C>A c.3353C>A (p.Pro1118His) c.3254C>A (p.Pro1085His) c.3668C>A (p.Pro1223His) | |
16 | g.9764033G>A | CA7896302 | GRIN2A | c.3511C>T (p.Pro1171Ser) c.3040C>T (p.Pro1014Ser) n.3104C>T c.*881C>T (n.*881C>T) c.3100C>T (p.Pro1034Ser) n.3150C>T c.3352C>T (p.Pro1118Ser) c.3253C>T (p.Pro1085Ser) c.3667C>T (p.Pro1223Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
16 | g.9764033G>C | CA394707462 | GRIN2A | c.3511C>G (p.Pro1171Ala) c.3040C>G (p.Pro1014Ala) n.3104C>G c.*881C>G (n.*881C>G) c.3100C>G (p.Pro1034Ala) n.3150C>G c.3352C>G (p.Pro1118Ala) c.3253C>G (p.Pro1085Ala) c.3667C>G (p.Pro1223Ala) | dbSNP gnomAD v4 |
16 | g.9764033G= | CA2206693021 | GRIN2A | c.3511C= (p.Pro1171=) c.3040C= (p.Pro1014=) n.3104C= c.*881C= (n.*881C=) c.3100C= (p.Pro1034=) n.3150C= c.3352C= (p.Pro1118=) c.3253C= (p.Pro1085=) c.3667C= (p.Pro1223=) | |
16 | g.9764033G>T | CA7896301 | GRIN2A | c.3511C>A (p.Pro1171Thr) c.3040C>A (p.Pro1014Thr) n.3104C>A c.*881C>A (n.*881C>A) c.3100C>A (p.Pro1034Thr) n.3150C>A c.3352C>A (p.Pro1118Thr) c.3253C>A (p.Pro1085Thr) c.3667C>A (p.Pro1223Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.9764034G>A | CA493693365 | GRIN2A | c.3510C>T (p.Asn1170=) c.3039C>T (p.Asn1013=) n.3103C>T c.*880C>T (n.*880C>T) c.3099C>T (p.Asn1033=) n.3149C>T c.3351C>T (p.Asn1117=) c.3252C>T (p.Asn1084=) c.3666C>T (p.Asn1222=) | dbSNP COSMIC |
16 | g.9764034G>C | CA394707463 | GRIN2A | c.3510C>G (p.Asn1170Lys) c.3039C>G (p.Asn1013Lys) n.3103C>G c.*880C>G (n.*880C>G) c.3099C>G (p.Asn1033Lys) n.3149C>G c.3351C>G (p.Asn1117Lys) c.3252C>G (p.Asn1084Lys) c.3666C>G (p.Asn1222Lys) | dbSNP gnomAD v4 |
16 | g.9764034G>T | CA394707464 | GRIN2A | c.3510C>A (p.Asn1170Lys) c.3039C>A (p.Asn1013Lys) n.3103C>A c.*880C>A (n.*880C>A) c.3099C>A (p.Asn1033Lys) n.3149C>A c.3351C>A (p.Asn1117Lys) c.3252C>A (p.Asn1084Lys) c.3666C>A (p.Asn1222Lys) | |
16 | g.9764034_9764035insCA | CA2520747057 | GRIN2A | c.3509_3510insTG (p.Pro1171AlafsTer24) c.3038_3039insTG (p.Pro1014AlafsTer24) n.3102_3103insTG c.*879_*880insTG (n.*879_*880insTG) c.3098_3099insTG (p.Pro1034AlafsTer24) n.3148_3149insTG c.3350_3351insTG (p.Pro1118AlafsTer24) c.3251_3252insTG (p.Pro1085AlafsTer24) c.3665_3666insTG (p.Pro1223AlafsTer24) | |
16 | g.9764034_9764035insGACTCCACGCTGCCAA | CA2805820127 | GRIN2A | c.3509_3510insTTGGCAGCGTGGAGTC (p.Pro1171TrpfsTer9) c.3038_3039insTTGGCAGCGTGGAGTC (p.Pro1014TrpfsTer9) n.3102_3103insTTGGCAGCGTGGAGTC c.*879_*880insTTGGCAGCGTGGAGTC (n.*879_*880insTTGGCAGCGTGGAGTC) c.3098_3099insTTGGCAGCGTGGAGTC (p.Pro1034TrpfsTer9) n.3148_3149insTTGGCAGCGTGGAGTC c.3350_3351insTTGGCAGCGTGGAGTC (p.Pro1118TrpfsTer9) c.3251_3252insTTGGCAGCGTGGAGTC (p.Pro1085TrpfsTer9) c.3665_3666insTTGGCAGCGTGGAGTC (p.Pro1223TrpfsTer9) | |
16 | g.9764035T>A | CA394707465 | GRIN2A | c.3509A>T (p.Asn1170Ile) c.3038A>T (p.Asn1013Ile) n.3102A>T c.*879A>T (n.*879A>T) c.3098A>T (p.Asn1033Ile) n.3148A>T c.3350A>T (p.Asn1117Ile) c.3251A>T (p.Asn1084Ile) c.3665A>T (p.Asn1222Ile) | ClinVar dbSNP |
16 | g.9764035T>C | CA394707466 | GRIN2A | c.3509A>G (p.Asn1170Ser) c.3038A>G (p.Asn1013Ser) n.3102A>G c.*879A>G (n.*879A>G) c.3098A>G (p.Asn1033Ser) n.3148A>G c.3350A>G (p.Asn1117Ser) c.3251A>G (p.Asn1084Ser) c.3665A>G (p.Asn1222Ser) | |
16 | g.9764035T>G | CA394707467 | GRIN2A | c.3509A>C (p.Asn1170Thr) c.3038A>C (p.Asn1013Thr) n.3102A>C c.*879A>C (n.*879A>C) c.3098A>C (p.Asn1033Thr) n.3148A>C c.3350A>C (p.Asn1117Thr) c.3251A>C (p.Asn1084Thr) c.3665A>C (p.Asn1222Thr) | dbSNP |
16 | g.9764036T>A | CA394707468 | GRIN2A | c.3508A>T (p.Asn1170Tyr) c.3037A>T (p.Asn1013Tyr) n.3101A>T c.*878A>T (n.*878A>T) c.3097A>T (p.Asn1033Tyr) n.3147A>T c.3349A>T (p.Asn1117Tyr) c.3250A>T (p.Asn1084Tyr) c.3664A>T (p.Asn1222Tyr) | dbSNP |
16 | g.9764036T>C | CA394707469 | GRIN2A | c.3508A>G (p.Asn1170Asp) c.3037A>G (p.Asn1013Asp) n.3101A>G c.*878A>G (n.*878A>G) c.3097A>G (p.Asn1033Asp) n.3147A>G c.3349A>G (p.Asn1117Asp) c.3250A>G (p.Asn1084Asp) c.3664A>G (p.Asn1222Asp) | dbSNP |
16 | g.9764036T>G | CA394707470 | GRIN2A | c.3508A>C (p.Asn1170His) c.3037A>C (p.Asn1013His) n.3101A>C c.*878A>C (n.*878A>C) c.3097A>C (p.Asn1033His) n.3147A>C c.3349A>C (p.Asn1117His) c.3250A>C (p.Asn1084His) c.3664A>C (p.Asn1222His) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.9764036T= | CA2206693022 | GRIN2A | c.3508A= (p.Asn1170=) c.3037A= (p.Asn1013=) n.3101A= c.*878A= (n.*878A=) c.3097A= (p.Asn1033=) n.3147A= c.3349A= (p.Asn1117=) c.3250A= (p.Asn1084=) c.3664A= (p.Asn1222=) | |
16 | g.9764037C>A | CA493693368 | GRIN2A | c.3507G>T (p.Arg1169=) c.3036G>T (p.Arg1012=) n.3100G>T c.*877G>T (n.*877G>T) c.3096G>T (p.Arg1032=) n.3146G>T c.3348G>T (p.Arg1116=) c.3249G>T (p.Arg1083=) c.3663G>T (p.Arg1221=) | |
16 | g.9764037C>G | CA493693369 | GRIN2A | c.3507G>C (p.Arg1169=) c.3036G>C (p.Arg1012=) n.3100G>C c.*877G>C (n.*877G>C) c.3096G>C (p.Arg1032=) n.3146G>C c.3348G>C (p.Arg1116=) c.3249G>C (p.Arg1083=) c.3663G>C (p.Arg1221=) | dbSNP |
16 | g.9764037C>T | CA493693370 | GRIN2A | c.3507G>A (p.Arg1169=) c.3036G>A (p.Arg1012=) n.3100G>A c.*877G>A (n.*877G>A) c.3096G>A (p.Arg1032=) n.3146G>A c.3348G>A (p.Arg1116=) c.3249G>A (p.Arg1083=) c.3663G>A (p.Arg1221=) | dbSNP gnomAD v4 |
16 | g.9764038C>A | CA394707471 | GRIN2A | c.3506G>T (p.Arg1169Leu) c.3035G>T (p.Arg1012Leu) n.3099G>T c.*876G>T (n.*876G>T) c.3095G>T (p.Arg1032Leu) n.3145G>T c.3347G>T (p.Arg1116Leu) c.3248G>T (p.Arg1083Leu) c.3662G>T (p.Arg1221Leu) | dbSNP |
16 | g.9764038C= | CA2206693023 | GRIN2A | c.3506G= (p.Arg1169=) c.3035G= (p.Arg1012=) n.3099G= c.*876G= (n.*876G=) c.3095G= (p.Arg1032=) n.3145G= c.3347G= (p.Arg1116=) c.3248G= (p.Arg1083=) c.3662G= (p.Arg1221=) | |
16 | g.9764038C>G | CA394707472 | GRIN2A | c.3506G>C (p.Arg1169Pro) c.3035G>C (p.Arg1012Pro) n.3099G>C c.*876G>C (n.*876G>C) c.3095G>C (p.Arg1032Pro) n.3145G>C c.3347G>C (p.Arg1116Pro) c.3248G>C (p.Arg1083Pro) c.3662G>C (p.Arg1221Pro) | dbSNP |
16 | g.9764038C>T | CA7896303 | GRIN2A | c.3506G>A (p.Arg1169Gln) c.3035G>A (p.Arg1012Gln) n.3099G>A c.*876G>A (n.*876G>A) c.3095G>A (p.Arg1032Gln) n.3145G>A c.3347G>A (p.Arg1116Gln) c.3248G>A (p.Arg1083Gln) c.3662G>A (p.Arg1221Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
16 | g.9764039G>A | CA7896304 | GRIN2A | c.3505C>T (p.Arg1169Trp) c.3034C>T (p.Arg1012Trp) n.3098C>T c.*875C>T (n.*875C>T) c.3094C>T (p.Arg1032Trp) n.3144C>T c.3346C>T (p.Arg1116Trp) c.3247C>T (p.Arg1083Trp) c.3661C>T (p.Arg1221Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
16 | g.9764039G>C | CA394707474 | GRIN2A | c.3505C>G (p.Arg1169Gly) c.3034C>G (p.Arg1012Gly) n.3098C>G c.*875C>G (n.*875C>G) c.3094C>G (p.Arg1032Gly) n.3144C>G c.3346C>G (p.Arg1116Gly) c.3247C>G (p.Arg1083Gly) c.3661C>G (p.Arg1221Gly) | ClinVar dbSNP |
16 | g.9764039G= | CA2206693024 | GRIN2A | c.3505C= (p.Arg1169=) c.3034C= (p.Arg1012=) n.3098C= c.*875C= (n.*875C=) c.3094C= (p.Arg1032=) n.3144C= c.3346C= (p.Arg1116=) c.3247C= (p.Arg1083=) c.3661C= (p.Arg1221=) | |
16 | g.9764039G>T | CA493693374 | GRIN2A | c.3505C>A (p.Arg1169=) c.3034C>A (p.Arg1012=) n.3098C>A c.*875C>A (n.*875C>A) c.3094C>A (p.Arg1032=) n.3144C>A c.3346C>A (p.Arg1116=) c.3247C>A (p.Arg1083=) c.3661C>A (p.Arg1221=) | dbSNP gnomAD v4 COSMIC |
16 | g.9764040G>A | CA277537199 | GRIN2A | c.3504C>T (p.Asn1168=) c.3033C>T (p.Asn1011=) n.3097C>T c.*874C>T (n.*874C>T) c.3093C>T (p.Asn1031=) n.3143C>T c.3345C>T (p.Asn1115=) c.3246C>T (p.Asn1082=) c.3660C>T (p.Asn1220=) | ClinVar dbSNP gnomAD v4 |
16 | g.9764040G>C | CA277537203 | GRIN2A | c.3504C>G (p.Asn1168Lys) c.3033C>G (p.Asn1011Lys) n.3097C>G c.*874C>G (n.*874C>G) c.3093C>G (p.Asn1031Lys) n.3143C>G c.3345C>G (p.Asn1115Lys) c.3246C>G (p.Asn1082Lys) c.3660C>G (p.Asn1220Lys) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.9764040G= | CA2206693025 | GRIN2A | c.3504C= (p.Asn1168=) c.3033C= (p.Asn1011=) n.3097C= c.*874C= (n.*874C=) c.3093C= (p.Asn1031=) n.3143C= c.3345C= (p.Asn1115=) c.3246C= (p.Asn1082=) c.3660C= (p.Asn1220=) | |
16 | g.9764040G>T | CA394707477 | GRIN2A | c.3504C>A (p.Asn1168Lys) c.3033C>A (p.Asn1011Lys) n.3097C>A c.*874C>A (n.*874C>A) c.3093C>A (p.Asn1031Lys) n.3143C>A c.3345C>A (p.Asn1115Lys) c.3246C>A (p.Asn1082Lys) c.3660C>A (p.Asn1220Lys) | gnomAD v4 |
16 | g.9764041T>A | CA394707484 | GRIN2A | c.3503A>T (p.Asn1168Ile) c.3032A>T (p.Asn1011Ile) n.3096A>T c.*873A>T (n.*873A>T) c.3092A>T (p.Asn1031Ile) n.3142A>T c.3344A>T (p.Asn1115Ile) c.3245A>T (p.Asn1082Ile) c.3659A>T (p.Asn1220Ile) | dbSNP |
16 | g.9764041T>C | CA394707481 | GRIN2A | c.3503A>G (p.Asn1168Ser) c.3032A>G (p.Asn1011Ser) n.3096A>G c.*873A>G (n.*873A>G) c.3092A>G (p.Asn1031Ser) n.3142A>G c.3344A>G (p.Asn1115Ser) c.3245A>G (p.Asn1082Ser) c.3659A>G (p.Asn1220Ser) | dbSNP |
16 | g.9764041T>G | CA394707482 | GRIN2A | c.3503A>C (p.Asn1168Thr) c.3032A>C (p.Asn1011Thr) n.3096A>C c.*873A>C (n.*873A>C) c.3092A>C (p.Asn1031Thr) n.3142A>C c.3344A>C (p.Asn1115Thr) c.3245A>C (p.Asn1082Thr) c.3659A>C (p.Asn1220Thr) | dbSNP |
16 | g.9764042T>A | CA394707487 | GRIN2A | c.3502A>T (p.Asn1168Tyr) c.3031A>T (p.Asn1011Tyr) n.3095A>T c.*872A>T (n.*872A>T) c.3091A>T (p.Asn1031Tyr) n.3141A>T c.3343A>T (p.Asn1115Tyr) c.3244A>T (p.Asn1082Tyr) c.3658A>T (p.Asn1220Tyr) | dbSNP |
16 | g.9764042T>C | CA394707489 | GRIN2A | c.3502A>G (p.Asn1168Asp) c.3031A>G (p.Asn1011Asp) n.3095A>G c.*872A>G (n.*872A>G) c.3091A>G (p.Asn1031Asp) n.3141A>G c.3343A>G (p.Asn1115Asp) c.3244A>G (p.Asn1082Asp) c.3658A>G (p.Asn1220Asp) | dbSNP |
16 | g.9764042T>G | CA394707490 | GRIN2A | c.3502A>C (p.Asn1168His) c.3031A>C (p.Asn1011His) n.3095A>C c.*872A>C (n.*872A>C) c.3091A>C (p.Asn1031His) n.3141A>C c.3343A>C (p.Asn1115His) c.3244A>C (p.Asn1082His) c.3658A>C (p.Asn1220His) | |
16 | g.9764043C>A | CA394707493 | GRIN2A | c.3501G>T (p.Met1167Ile) c.3030G>T (p.Met1010Ile) n.3094G>T c.*871G>T (n.*871G>T) c.3090G>T (p.Met1030Ile) n.3140G>T c.3342G>T (p.Met1114Ile) c.3243G>T (p.Met1081Ile) c.3657G>T (p.Met1219Ile) | dbSNP |
16 | g.9764043C>G | CA394707495 | GRIN2A | c.3501G>C (p.Met1167Ile) c.3030G>C (p.Met1010Ile) n.3094G>C c.*871G>C (n.*871G>C) c.3090G>C (p.Met1030Ile) n.3140G>C c.3342G>C (p.Met1114Ile) c.3243G>C (p.Met1081Ile) c.3657G>C (p.Met1219Ile) | dbSNP |
16 | g.9764043C>T | CA394707496 | GRIN2A | c.3501G>A (p.Met1167Ile) c.3030G>A (p.Met1010Ile) n.3094G>A c.*871G>A (n.*871G>A) c.3090G>A (p.Met1030Ile) n.3140G>A c.3342G>A (p.Met1114Ile) c.3243G>A (p.Met1081Ile) c.3657G>A (p.Met1219Ile) | dbSNP |
16 | g.9764044A>C | CA394707499 | GRIN2A | c.3500T>G (p.Met1167Arg) c.3029T>G (p.Met1010Arg) n.3093T>G c.*870T>G (n.*870T>G) c.3089T>G (p.Met1030Arg) n.3139T>G c.3341T>G (p.Met1114Arg) c.3242T>G (p.Met1081Arg) c.3656T>G (p.Met1219Arg) | |
16 | g.9764044A>G | CA394707501 | GRIN2A | c.3500T>C (p.Met1167Thr) c.3029T>C (p.Met1010Thr) n.3093T>C c.*870T>C (n.*870T>C) c.3089T>C (p.Met1030Thr) n.3139T>C c.3341T>C (p.Met1114Thr) c.3242T>C (p.Met1081Thr) c.3656T>C (p.Met1219Thr) | gnomAD v4 |
16 | g.9764044A>T | CA394707503 | GRIN2A | c.3500T>A (p.Met1167Lys) c.3029T>A (p.Met1010Lys) n.3093T>A c.*870T>A (n.*870T>A) c.3089T>A (p.Met1030Lys) n.3139T>A c.3341T>A (p.Met1114Lys) c.3242T>A (p.Met1081Lys) c.3656T>A (p.Met1219Lys) | ClinVar dbSNP gnomAD v4 |
16 | g.9764045T>A | CA394707505 | GRIN2A | c.3499A>T (p.Met1167Leu) c.3028A>T (p.Met1010Leu) n.3092A>T c.*869A>T (n.*869A>T) c.3088A>T (p.Met1030Leu) n.3138A>T c.3340A>T (p.Met1114Leu) c.3241A>T (p.Met1081Leu) c.3655A>T (p.Met1219Leu) | dbSNP |
16 | g.9764045T>C | CA394707508 | GRIN2A | c.3499A>G (p.Met1167Val) c.3028A>G (p.Met1010Val) n.3092A>G c.*869A>G (n.*869A>G) c.3088A>G (p.Met1030Val) n.3138A>G c.3340A>G (p.Met1114Val) c.3241A>G (p.Met1081Val) c.3655A>G (p.Met1219Val) | gnomAD v4 |
16 | g.9764045T>G | CA394707510 | GRIN2A | c.3499A>C (p.Met1167Leu) c.3028A>C (p.Met1010Leu) n.3092A>C c.*869A>C (n.*869A>C) c.3088A>C (p.Met1030Leu) n.3138A>C c.3340A>C (p.Met1114Leu) c.3241A>C (p.Met1081Leu) c.3655A>C (p.Met1219Leu) | |
16 | g.9764046T>A | CA493693379 | GRIN2A | c.3498A>T (p.Pro1166=) c.3027A>T (p.Pro1009=) n.3091A>T c.*868A>T (n.*868A>T) c.3087A>T (p.Pro1029=) n.3137A>T c.3339A>T (p.Pro1113=) c.3240A>T (p.Pro1080=) c.3654A>T (p.Pro1218=) | |
16 | g.9764046T>C | CA493693381 | GRIN2A | c.3498A>G (p.Pro1166=) c.3027A>G (p.Pro1009=) n.3091A>G c.*868A>G (n.*868A>G) c.3087A>G (p.Pro1029=) n.3137A>G c.3339A>G (p.Pro1113=) c.3240A>G (p.Pro1080=) c.3654A>G (p.Pro1218=) | |
16 | g.9764046T>G | CA493693382 | GRIN2A | c.3498A>C (p.Pro1166=) c.3027A>C (p.Pro1009=) n.3091A>C c.*868A>C (n.*868A>C) c.3087A>C (p.Pro1029=) n.3137A>C c.3339A>C (p.Pro1113=) c.3240A>C (p.Pro1080=) c.3654A>C (p.Pro1218=) | |
16 | g.9764047G>A | CA394707516 | GRIN2A | c.3497C>T (p.Pro1166Leu) c.3026C>T (p.Pro1009Leu) n.3090C>T c.*867C>T (n.*867C>T) c.3086C>T (p.Pro1029Leu) n.3136C>T c.3338C>T (p.Pro1113Leu) c.3239C>T (p.Pro1080Leu) c.3653C>T (p.Pro1218Leu) | dbSNP gnomAD v4 |
16 | g.9764047G>C | CA394707515 | GRIN2A | c.3497C>G (p.Pro1166Arg) c.3026C>G (p.Pro1009Arg) n.3090C>G c.*867C>G (n.*867C>G) c.3086C>G (p.Pro1029Arg) n.3136C>G c.3338C>G (p.Pro1113Arg) c.3239C>G (p.Pro1080Arg) c.3653C>G (p.Pro1218Arg) | dbSNP |
16 | g.9764047G>T | CA394707513 | GRIN2A | c.3497C>A (p.Pro1166Gln) c.3026C>A (p.Pro1009Gln) n.3090C>A c.*867C>A (n.*867C>A) c.3086C>A (p.Pro1029Gln) n.3136C>A c.3338C>A (p.Pro1113Gln) c.3239C>A (p.Pro1080Gln) c.3653C>A (p.Pro1218Gln) | dbSNP |
16 | g.9764048G>A | CA394707521 | GRIN2A | c.3496C>T (p.Pro1166Ser) c.3025C>T (p.Pro1009Ser) n.3089C>T c.*866C>T (n.*866C>T) c.3085C>T (p.Pro1029Ser) n.3135C>T c.3337C>T (p.Pro1113Ser) c.3238C>T (p.Pro1080Ser) c.3652C>T (p.Pro1218Ser) | dbSNP |
16 | g.9764048G>C | CA394707519 | GRIN2A | c.3496C>G (p.Pro1166Ala) c.3025C>G (p.Pro1009Ala) n.3089C>G c.*866C>G (n.*866C>G) c.3085C>G (p.Pro1029Ala) n.3135C>G c.3337C>G (p.Pro1113Ala) c.3238C>G (p.Pro1080Ala) c.3652C>G (p.Pro1218Ala) | dbSNP |
16 | g.9764048G>T | CA394707523 | GRIN2A | c.3496C>A (p.Pro1166Thr) c.3025C>A (p.Pro1009Thr) n.3089C>A c.*866C>A (n.*866C>A) c.3085C>A (p.Pro1029Thr) n.3135C>A c.3337C>A (p.Pro1113Thr) c.3238C>A (p.Pro1080Thr) c.3652C>A (p.Pro1218Thr) | dbSNP |
16 | g.9764049C>A | CA493693385 | GRIN2A | c.3495G>T (p.Leu1165=) c.3024G>T (p.Leu1008=) n.3088G>T c.*865G>T (n.*865G>T) c.3084G>T (p.Leu1028=) n.3134G>T c.3336G>T (p.Leu1112=) c.3237G>T (p.Leu1079=) c.3651G>T (p.Leu1217=) | dbSNP |
16 | g.9764049C>G | CA493693386 | GRIN2A | c.3495G>C (p.Leu1165=) c.3024G>C (p.Leu1008=) n.3088G>C c.*865G>C (n.*865G>C) c.3084G>C (p.Leu1028=) n.3134G>C c.3336G>C (p.Leu1112=) c.3237G>C (p.Leu1079=) c.3651G>C (p.Leu1217=) | dbSNP |
16 | g.9764049C>T | CA493693388 | GRIN2A | c.3495G>A (p.Leu1165=) c.3024G>A (p.Leu1008=) n.3088G>A c.*865G>A (n.*865G>A) c.3084G>A (p.Leu1028=) n.3134G>A c.3336G>A (p.Leu1112=) c.3237G>A (p.Leu1079=) c.3651G>A (p.Leu1217=) | dbSNP |
16 | g.9764050A>C | CA394707525 | GRIN2A | c.3494T>G (p.Leu1165Arg) c.3023T>G (p.Leu1008Arg) n.3087T>G c.*864T>G (n.*864T>G) c.3083T>G (p.Leu1028Arg) n.3133T>G c.3335T>G (p.Leu1112Arg) c.3236T>G (p.Leu1079Arg) c.3650T>G (p.Leu1217Arg) | |
16 | g.9764050A>G | CA394707529 | GRIN2A | c.3494T>C (p.Leu1165Pro) c.3023T>C (p.Leu1008Pro) n.3087T>C c.*864T>C (n.*864T>C) c.3083T>C (p.Leu1028Pro) n.3133T>C c.3335T>C (p.Leu1112Pro) c.3236T>C (p.Leu1079Pro) c.3650T>C (p.Leu1217Pro) | |
16 | g.9764050A>T | CA394707527 | GRIN2A | c.3494T>A (p.Leu1165Gln) c.3023T>A (p.Leu1008Gln) n.3087T>A c.*864T>A (n.*864T>A) c.3083T>A (p.Leu1028Gln) n.3133T>A c.3335T>A (p.Leu1112Gln) c.3236T>A (p.Leu1079Gln) c.3650T>A (p.Leu1217Gln) | dbSNP |
16 | g.9764051G>A | CA493693391 | GRIN2A | c.3493C>T (p.Leu1165=) c.3022C>T (p.Leu1008=) n.3086C>T c.*863C>T (n.*863C>T) c.3082C>T (p.Leu1028=) n.3132C>T c.3334C>T (p.Leu1112=) c.3235C>T (p.Leu1079=) c.3649C>T (p.Leu1217=) | ClinVar dbSNP gnomAD v4 |
16 | g.9764051G>C | CA394707532 | GRIN2A | c.3493C>G (p.Leu1165Val) c.3022C>G (p.Leu1008Val) n.3086C>G c.*863C>G (n.*863C>G) c.3082C>G (p.Leu1028Val) n.3132C>G c.3334C>G (p.Leu1112Val) c.3235C>G (p.Leu1079Val) c.3649C>G (p.Leu1217Val) | dbSNP |
16 | g.9764051G>T | CA394707533 | GRIN2A | c.3493C>A (p.Leu1165Met) c.3022C>A (p.Leu1008Met) n.3086C>A c.*863C>A (n.*863C>A) c.3082C>A (p.Leu1028Met) n.3132C>A c.3334C>A (p.Leu1112Met) c.3235C>A (p.Leu1079Met) c.3649C>A (p.Leu1217Met) | dbSNP gnomAD v4 |
16 | g.9764052C>A | CA493693395 | GRIN2A | c.3492G>T (p.Thr1164=) c.3021G>T (p.Thr1007=) n.3085G>T c.*862G>T (n.*862G>T) c.3081G>T (p.Thr1027=) n.3131G>T c.3333G>T (p.Thr1111=) c.3234G>T (p.Thr1078=) c.3648G>T (p.Thr1216=) | |
16 | g.9764052C= | CA2206693026 | GRIN2A | c.3492G= (p.Thr1164=) c.3021G= (p.Thr1007=) n.3085G= c.*862G= (n.*862G=) c.3081G= (p.Thr1027=) n.3131G= c.3333G= (p.Thr1111=) c.3234G= (p.Thr1078=) c.3648G= (p.Thr1216=) | |
16 | g.9764052C>G | CA493693394 | GRIN2A | c.3492G>C (p.Thr1164=) c.3021G>C (p.Thr1007=) n.3085G>C c.*862G>C (n.*862G>C) c.3081G>C (p.Thr1027=) n.3131G>C c.3333G>C (p.Thr1111=) c.3234G>C (p.Thr1078=) c.3648G>C (p.Thr1216=) | dbSNP |
16 | g.9764052C>T | CA493693393 | GRIN2A | c.3492G>A (p.Thr1164=) c.3021G>A (p.Thr1007=) n.3085G>A c.*862G>A (n.*862G>A) c.3081G>A (p.Thr1027=) n.3131G>A c.3333G>A (p.Thr1111=) c.3234G>A (p.Thr1078=) c.3648G>A (p.Thr1216=) | ClinVar dbSNP gnomAD v4 |
16 | g.9764053G>A | CA394707536 | GRIN2A | c.3491C>T (p.Thr1164Met) c.3020C>T (p.Thr1007Met) n.3084C>T c.*861C>T (n.*861C>T) c.3080C>T (p.Thr1027Met) n.3130C>T c.3332C>T (p.Thr1111Met) c.3233C>T (p.Thr1078Met) c.3647C>T (p.Thr1216Met) | ClinVar dbSNP gnomAD v4 COSMIC |
16 | g.9764053G>C | CA394707537 | GRIN2A | c.3491C>G (p.Thr1164Arg) c.3020C>G (p.Thr1007Arg) n.3084C>G c.*861C>G (n.*861C>G) c.3080C>G (p.Thr1027Arg) n.3130C>G c.3332C>G (p.Thr1111Arg) c.3233C>G (p.Thr1078Arg) c.3647C>G (p.Thr1216Arg) | dbSNP gnomAD v4 |
16 | g.9764053G>T | CA394707539 | GRIN2A | c.3491C>A (p.Thr1164Lys) c.3020C>A (p.Thr1007Lys) n.3084C>A c.*861C>A (n.*861C>A) c.3080C>A (p.Thr1027Lys) n.3130C>A c.3332C>A (p.Thr1111Lys) c.3233C>A (p.Thr1078Lys) c.3647C>A (p.Thr1216Lys) | |
16 | g.9764054T>A | CA394707542 | GRIN2A | c.3490A>T (p.Thr1164Ser) c.3019A>T (p.Thr1007Ser) n.3083A>T c.*860A>T (n.*860A>T) c.3079A>T (p.Thr1027Ser) n.3129A>T c.3331A>T (p.Thr1111Ser) c.3232A>T (p.Thr1078Ser) c.3646A>T (p.Thr1216Ser) | |
16 | g.9764054T>C | CA394707543 | GRIN2A | c.3490A>G (p.Thr1164Ala) c.3019A>G (p.Thr1007Ala) n.3083A>G c.*860A>G (n.*860A>G) c.3079A>G (p.Thr1027Ala) n.3129A>G c.3331A>G (p.Thr1111Ala) c.3232A>G (p.Thr1078Ala) c.3646A>G (p.Thr1216Ala) | |
16 | g.9764054T>G | CA394707544 | GRIN2A | c.3490A>C (p.Thr1164Pro) c.3019A>C (p.Thr1007Pro) n.3083A>C c.*860A>C (n.*860A>C) c.3079A>C (p.Thr1027Pro) n.3129A>C c.3331A>C (p.Thr1111Pro) c.3232A>C (p.Thr1078Pro) c.3646A>C (p.Thr1216Pro) | |
16 | g.9764055G>A | CA493693401 | GRIN2A | c.3489C>T (p.Ser1163=) c.3018C>T (p.Ser1006=) n.3082C>T c.*859C>T (n.*859C>T) c.3078C>T (p.Ser1026=) n.3128C>T c.3330C>T (p.Ser1110=) c.3231C>T (p.Ser1077=) c.3645C>T (p.Ser1215=) | dbSNP gnomAD v4 |
16 | g.9764055G>C | CA7896305 | GRIN2A | c.3489C>G (p.Ser1163=) c.3018C>G (p.Ser1006=) n.3082C>G c.*859C>G (n.*859C>G) c.3078C>G (p.Ser1026=) n.3128C>G c.3330C>G (p.Ser1110=) c.3231C>G (p.Ser1077=) c.3645C>G (p.Ser1215=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.9764055G= | CA2206693027 | GRIN2A | c.3489C= (p.Ser1163=) c.3018C= (p.Ser1006=) n.3082C= c.*859C= (n.*859C=) c.3078C= (p.Ser1026=) n.3128C= c.3330C= (p.Ser1110=) c.3231C= (p.Ser1077=) c.3645C= (p.Ser1215=) | |
16 | g.9764055G>T | CA493693400 | GRIN2A | c.3489C>A (p.Ser1163=) c.3018C>A (p.Ser1006=) n.3082C>A c.*859C>A (n.*859C>A) c.3078C>A (p.Ser1026=) n.3128C>A c.3330C>A (p.Ser1110=) c.3231C>A (p.Ser1077=) c.3645C>A (p.Ser1215=) | |
16 | g.9764056G>A | CA394707548 | GRIN2A | c.3488C>T (p.Ser1163Phe) c.3017C>T (p.Ser1006Phe) n.3081C>T c.*858C>T (n.*858C>T) c.3077C>T (p.Ser1026Phe) n.3127C>T c.3329C>T (p.Ser1110Phe) c.3230C>T (p.Ser1077Phe) c.3644C>T (p.Ser1215Phe) | dbSNP |
16 | g.9764056G>C | CA394707550 | GRIN2A | c.3488C>G (p.Ser1163Cys) c.3017C>G (p.Ser1006Cys) n.3081C>G c.*858C>G (n.*858C>G) c.3077C>G (p.Ser1026Cys) n.3127C>G c.3329C>G (p.Ser1110Cys) c.3230C>G (p.Ser1077Cys) c.3644C>G (p.Ser1215Cys) | dbSNP |
16 | g.9764056G= | CA2206693028 | GRIN2A | c.3488C= (p.Ser1163=) c.3017C= (p.Ser1006=) n.3081C= c.*858C= (n.*858C=) c.3077C= (p.Ser1026=) n.3127C= c.3329C= (p.Ser1110=) c.3230C= (p.Ser1077=) c.3644C= (p.Ser1215=) | |
16 | g.9764056G>T | CA394707551 | GRIN2A | c.3488C>A (p.Ser1163Tyr) c.3017C>A (p.Ser1006Tyr) n.3081C>A c.*858C>A (n.*858C>A) c.3077C>A (p.Ser1026Tyr) n.3127C>A c.3329C>A (p.Ser1110Tyr) c.3230C>A (p.Ser1077Tyr) c.3644C>A (p.Ser1215Tyr) | dbSNP |
16 | g.9764057A>C | CA394707558 | GRIN2A | c.3487T>G (p.Ser1163Ala) c.3016T>G (p.Ser1006Ala) n.3080T>G c.*857T>G (n.*857T>G) c.3076T>G (p.Ser1026Ala) n.3126T>G c.3328T>G (p.Ser1110Ala) c.3229T>G (p.Ser1077Ala) c.3643T>G (p.Ser1215Ala) | |
16 | g.9764057A>G | CA394707556 | GRIN2A | c.3487T>C (p.Ser1163Pro) c.3016T>C (p.Ser1006Pro) n.3080T>C c.*857T>C (n.*857T>C) c.3076T>C (p.Ser1026Pro) n.3126T>C c.3328T>C (p.Ser1110Pro) c.3229T>C (p.Ser1077Pro) c.3643T>C (p.Ser1215Pro) | dbSNP |
16 | g.9764057A>T | CA394707554 | GRIN2A | c.3487T>A (p.Ser1163Thr) c.3016T>A (p.Ser1006Thr) n.3080T>A c.*857T>A (n.*857T>A) c.3076T>A (p.Ser1026Thr) n.3126T>A c.3328T>A (p.Ser1110Thr) c.3229T>A (p.Ser1077Thr) c.3643T>A (p.Ser1215Thr) | dbSNP |
16 | g.9764058G>A | CA493693410 | GRIN2A | c.3486C>T (p.Asp1162=) c.3015C>T (p.Asp1005=) n.3079C>T c.*856C>T (n.*856C>T) c.3075C>T (p.Asp1025=) n.3125C>T c.3327C>T (p.Asp1109=) c.3228C>T (p.Asp1076=) c.3642C>T (p.Asp1214=) | dbSNP |
16 | g.9764058G>C | CA394707561 | GRIN2A | c.3486C>G (p.Asp1162Glu) c.3015C>G (p.Asp1005Glu) n.3079C>G c.*856C>G (n.*856C>G) c.3075C>G (p.Asp1025Glu) n.3125C>G c.3327C>G (p.Asp1109Glu) c.3228C>G (p.Asp1076Glu) c.3642C>G (p.Asp1214Glu) | dbSNP |
16 | g.9764058G= | CA2206693029 | GRIN2A | c.3486C= (p.Asp1162=) c.3015C= (p.Asp1005=) n.3079C= c.*856C= (n.*856C=) c.3075C= (p.Asp1025=) n.3125C= c.3327C= (p.Asp1109=) c.3228C= (p.Asp1076=) c.3642C= (p.Asp1214=) | |
16 | g.9764058G>T | CA394707562 | GRIN2A | c.3486C>A (p.Asp1162Glu) c.3015C>A (p.Asp1005Glu) n.3079C>A c.*856C>A (n.*856C>A) c.3075C>A (p.Asp1025Glu) n.3125C>A c.3327C>A (p.Asp1109Glu) c.3228C>A (p.Asp1076Glu) c.3642C>A (p.Asp1214Glu) | |
16 | g.9764059T>A | CA394707566 | GRIN2A | c.3485A>T (p.Asp1162Val) c.3014A>T (p.Asp1005Val) n.3078A>T c.*855A>T (n.*855A>T) c.3074A>T (p.Asp1025Val) n.3124A>T c.3326A>T (p.Asp1109Val) c.3227A>T (p.Asp1076Val) c.3641A>T (p.Asp1214Val) | dbSNP gnomAD v4 COSMIC |
16 | g.9764059T>C | CA394707568 | GRIN2A | c.3485A>G (p.Asp1162Gly) c.3014A>G (p.Asp1005Gly) n.3078A>G c.*855A>G (n.*855A>G) c.3074A>G (p.Asp1025Gly) n.3124A>G c.3326A>G (p.Asp1109Gly) c.3227A>G (p.Asp1076Gly) c.3641A>G (p.Asp1214Gly) | ClinVar |
16 | g.9764059T>G | CA394707570 | GRIN2A | c.3485A>C (p.Asp1162Ala) c.3014A>C (p.Asp1005Ala) n.3078A>C c.*855A>C (n.*855A>C) c.3074A>C (p.Asp1025Ala) n.3124A>C c.3326A>C (p.Asp1109Ala) c.3227A>C (p.Asp1076Ala) c.3641A>C (p.Asp1214Ala) | |
16 | g.9764060C>A | CA394707573 | GRIN2A | c.3484G>T (p.Asp1162Tyr) c.3013G>T (p.Asp1005Tyr) n.3077G>T c.*854G>T (n.*854G>T) c.3073G>T (p.Asp1025Tyr) n.3123G>T c.3325G>T (p.Asp1109Tyr) c.3226G>T (p.Asp1076Tyr) c.3640G>T (p.Asp1214Tyr) | dbSNP |
16 | g.9764060C= | CA2206693030 | GRIN2A | c.3484G= (p.Asp1162=) c.3013G= (p.Asp1005=) n.3077G= c.*854G= (n.*854G=) c.3073G= (p.Asp1025=) n.3123G= c.3325G= (p.Asp1109=) c.3226G= (p.Asp1076=) c.3640G= (p.Asp1214=) | |
16 | g.9764060C>G | CA394707575 | GRIN2A | c.3484G>C (p.Asp1162His) c.3013G>C (p.Asp1005His) n.3077G>C c.*854G>C (n.*854G>C) c.3073G>C (p.Asp1025His) n.3123G>C c.3325G>C (p.Asp1109His) c.3226G>C (p.Asp1076His) c.3640G>C (p.Asp1214His) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.9764060C>T | CA394707576 | GRIN2A | c.3484G>A (p.Asp1162Asn) c.3013G>A (p.Asp1005Asn) n.3077G>A c.*854G>A (n.*854G>A) c.3073G>A (p.Asp1025Asn) n.3123G>A c.3325G>A (p.Asp1109Asn) c.3226G>A (p.Asp1076Asn) c.3640G>A (p.Asp1214Asn) | dbSNP COSMIC |
16 | g.9764061C>A | CA493693412 | GRIN2A | c.3483G>T (p.Gly1161=) c.3012G>T (p.Gly1004=) n.3076G>T c.*853G>T (n.*853G>T) c.3072G>T (p.Gly1024=) n.3122G>T c.3324G>T (p.Gly1108=) c.3225G>T (p.Gly1075=) c.3639G>T (p.Gly1213=) | dbSNP |
16 | g.9764061C= | CA2206693031 | GRIN2A | c.3483G= (p.Gly1161=) c.3012G= (p.Gly1004=) n.3076G= c.*853G= (n.*853G=) c.3072G= (p.Gly1024=) n.3122G= c.3324G= (p.Gly1108=) c.3225G= (p.Gly1075=) c.3639G= (p.Gly1213=) | |
16 | g.9764061C>G | CA7896307 | GRIN2A | c.3483G>C (p.Gly1161=) c.3012G>C (p.Gly1004=) n.3076G>C c.*853G>C (n.*853G>C) c.3072G>C (p.Gly1024=) n.3122G>C c.3324G>C (p.Gly1108=) c.3225G>C (p.Gly1075=) c.3639G>C (p.Gly1213=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.9764061C>T | CA7896306 | GRIN2A | c.3483G>A (p.Gly1161=) c.3012G>A (p.Gly1004=) n.3076G>A c.*853G>A (n.*853G>A) c.3072G>A (p.Gly1024=) n.3122G>A c.3324G>A (p.Gly1108=) c.3225G>A (p.Gly1075=) c.3639G>A (p.Gly1213=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.9764062C>A | CA394707580 | GRIN2A | c.3482G>T (p.Gly1161Val) c.3011G>T (p.Gly1004Val) n.3075G>T c.*852G>T (n.*852G>T) c.3071G>T (p.Gly1024Val) n.3121G>T c.3323G>T (p.Gly1108Val) c.3224G>T (p.Gly1075Val) c.3638G>T (p.Gly1213Val) | dbSNP |
16 | g.9764062C= | CA2206693032 | GRIN2A | c.3482G= (p.Gly1161=) c.3011G= (p.Gly1004=) n.3075G= c.*852G= (n.*852G=) c.3071G= (p.Gly1024=) n.3121G= c.3323G= (p.Gly1108=) c.3224G= (p.Gly1075=) c.3638G= (p.Gly1213=) | |
16 | g.9764062C>G | CA394707581 | GRIN2A | c.3482G>C (p.Gly1161Ala) c.3011G>C (p.Gly1004Ala) n.3075G>C c.*852G>C (n.*852G>C) c.3071G>C (p.Gly1024Ala) n.3121G>C c.3323G>C (p.Gly1108Ala) c.3224G>C (p.Gly1075Ala) c.3638G>C (p.Gly1213Ala) | ClinVar dbSNP gnomAD v4 |
16 | g.9764062C>T | CA394707583 | GRIN2A | c.3482G>A (p.Gly1161Glu) c.3011G>A (p.Gly1004Glu) n.3075G>A c.*852G>A (n.*852G>A) c.3071G>A (p.Gly1024Glu) n.3121G>A c.3323G>A (p.Gly1108Glu) c.3224G>A (p.Gly1075Glu) c.3638G>A (p.Gly1213Glu) | ClinVar dbSNP |
16 | g.9764063C>A | CA394707585 | GRIN2A | c.3481G>T (p.Gly1161Trp) c.3010G>T (p.Gly1004Trp) n.3074G>T c.*851G>T (n.*851G>T) c.3070G>T (p.Gly1024Trp) n.3120G>T c.3322G>T (p.Gly1108Trp) c.3223G>T (p.Gly1075Trp) c.3637G>T (p.Gly1213Trp) | dbSNP gnomAD v4 |
16 | g.9764063C>G | CA394707587 | GRIN2A | c.3481G>C (p.Gly1161Arg) c.3010G>C (p.Gly1004Arg) n.3074G>C c.*851G>C (n.*851G>C) c.3070G>C (p.Gly1024Arg) n.3120G>C c.3322G>C (p.Gly1108Arg) c.3223G>C (p.Gly1075Arg) c.3637G>C (p.Gly1213Arg) | dbSNP |
16 | g.9764063C>T | CA394707584 | GRIN2A | c.3481G>A (p.Gly1161Arg) c.3010G>A (p.Gly1004Arg) n.3074G>A c.*851G>A (n.*851G>A) c.3070G>A (p.Gly1024Arg) n.3120G>A c.3322G>A (p.Gly1108Arg) c.3223G>A (p.Gly1075Arg) c.3637G>A (p.Gly1213Arg) | dbSNP gnomAD v4 COSMIC |
16 | g.9764064C>A | CA394707589 | GRIN2A | c.3480G>T (p.Lys1160Asn) c.3009G>T (p.Lys1003Asn) n.3073G>T c.*850G>T (n.*850G>T) c.3069G>T (p.Lys1023Asn) n.3119G>T c.3321G>T (p.Lys1107Asn) c.3222G>T (p.Lys1074Asn) c.3636G>T (p.Lys1212Asn) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.9764064C= | CA2206693033 | GRIN2A | c.3480G= (p.Lys1160=) c.3009G= (p.Lys1003=) n.3073G= c.*850G= (n.*850G=) c.3069G= (p.Lys1023=) n.3119G= c.3321G= (p.Lys1107=) c.3222G= (p.Lys1074=) c.3636G= (p.Lys1212=) | |
16 | g.9764064C>G | CA394707596 | GRIN2A | c.3480G>C (p.Lys1160Asn) c.3009G>C (p.Lys1003Asn) n.3073G>C c.*850G>C (n.*850G>C) c.3069G>C (p.Lys1023Asn) n.3119G>C c.3321G>C (p.Lys1107Asn) c.3222G>C (p.Lys1074Asn) c.3636G>C (p.Lys1212Asn) | ClinVar dbSNP |
16 | g.9764064C>T | CA493693417 | GRIN2A | c.3480G>A (p.Lys1160=) c.3009G>A (p.Lys1003=) n.3073G>A c.*850G>A (n.*850G>A) c.3069G>A (p.Lys1023=) n.3119G>A c.3321G>A (p.Lys1107=) c.3222G>A (p.Lys1074=) c.3636G>A (p.Lys1212=) | dbSNP |
16 | g.9764065T>A | CA394707599 | GRIN2A | c.3479A>T (p.Lys1160Met) c.3008A>T (p.Lys1003Met) n.3072A>T c.*849A>T (n.*849A>T) c.3068A>T (p.Lys1023Met) n.3118A>T c.3320A>T (p.Lys1107Met) c.3221A>T (p.Lys1074Met) c.3635A>T (p.Lys1212Met) | dbSNP |
16 | g.9764065T>C | CA394707601 | GRIN2A | c.3479A>G (p.Lys1160Arg) c.3008A>G (p.Lys1003Arg) n.3072A>G c.*849A>G (n.*849A>G) c.3068A>G (p.Lys1023Arg) n.3118A>G c.3320A>G (p.Lys1107Arg) c.3221A>G (p.Lys1074Arg) c.3635A>G (p.Lys1212Arg) | dbSNP |
16 | g.9764065T>G | CA394707603 | GRIN2A | c.3479A>C (p.Lys1160Thr) c.3008A>C (p.Lys1003Thr) n.3072A>C c.*849A>C (n.*849A>C) c.3068A>C (p.Lys1023Thr) n.3118A>C c.3320A>C (p.Lys1107Thr) c.3221A>C (p.Lys1074Thr) c.3635A>C (p.Lys1212Thr) | |
16 | g.9764066T>A | CA394707605 | GRIN2A | c.3478A>T (p.Lys1160Ter) c.3007A>T (p.Lys1003Ter) n.3071A>T c.*848A>T (n.*848A>T) c.3067A>T (p.Lys1023Ter) n.3117A>T c.3319A>T (p.Lys1107Ter) c.3220A>T (p.Lys1074Ter) c.3634A>T (p.Lys1212Ter) | dbSNP |
16 | g.9764066T>C | CA394707606 | GRIN2A | c.3478A>G (p.Lys1160Glu) c.3007A>G (p.Lys1003Glu) n.3071A>G c.*848A>G (n.*848A>G) c.3067A>G (p.Lys1023Glu) n.3117A>G c.3319A>G (p.Lys1107Glu) c.3220A>G (p.Lys1074Glu) c.3634A>G (p.Lys1212Glu) | dbSNP |
16 | g.9764066T>G | CA7896308 | GRIN2A | c.3478A>C (p.Lys1160Gln) c.3007A>C (p.Lys1003Gln) n.3071A>C c.*848A>C (n.*848A>C) c.3067A>C (p.Lys1023Gln) n.3117A>C c.3319A>C (p.Lys1107Gln) c.3220A>C (p.Lys1074Gln) c.3634A>C (p.Lys1212Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.9764066T= | CA2206693034 | GRIN2A | c.3478A= (p.Lys1160=) c.3007A= (p.Lys1003=) n.3071A= c.*848A= (n.*848A=) c.3067A= (p.Lys1023=) n.3117A= c.3319A= (p.Lys1107=) c.3220A= (p.Lys1074=) c.3634A= (p.Lys1212=) | |
16 | g.9764067G>A | CA493693420 | GRIN2A | c.3477C>T (p.Arg1159=) c.3006C>T (p.Arg1002=) n.3070C>T c.*847C>T (n.*847C>T) c.3066C>T (p.Arg1022=) n.3116C>T c.3318C>T (p.Arg1106=) c.3219C>T (p.Arg1073=) c.3633C>T (p.Arg1211=) | |
16 | g.9764067G>C | CA493693422 | GRIN2A | c.3477C>G (p.Arg1159=) c.3006C>G (p.Arg1002=) n.3070C>G c.*847C>G (n.*847C>G) c.3066C>G (p.Arg1022=) n.3116C>G c.3318C>G (p.Arg1106=) c.3219C>G (p.Arg1073=) c.3633C>G (p.Arg1211=) | |
16 | g.9764067G>T | CA493693425 | GRIN2A | c.3477C>A (p.Arg1159=) c.3006C>A (p.Arg1002=) n.3070C>A c.*847C>A (n.*847C>A) c.3066C>A (p.Arg1022=) n.3116C>A c.3318C>A (p.Arg1106=) c.3219C>A (p.Arg1073=) c.3633C>A (p.Arg1211=) | |
16 | g.9764068C>A | CA7896311 | GRIN2A | c.3476G>T (p.Arg1159Leu) c.3005G>T (p.Arg1002Leu) n.3069G>T c.*846G>T (n.*846G>T) c.3065G>T (p.Arg1022Leu) n.3115G>T c.3317G>T (p.Arg1106Leu) c.3218G>T (p.Arg1073Leu) c.3632G>T (p.Arg1211Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.9764068C= | CA2206693035 | GRIN2A | c.3476G= (p.Arg1159=) c.3005G= (p.Arg1002=) n.3069G= c.*846G= (n.*846G=) c.3065G= (p.Arg1022=) n.3115G= c.3317G= (p.Arg1106=) c.3218G= (p.Arg1073=) c.3632G= (p.Arg1211=) | |
16 | g.9764068C>G | CA7896310 | GRIN2A | c.3476G>C (p.Arg1159Pro) c.3005G>C (p.Arg1002Pro) n.3069G>C c.*846G>C (n.*846G>C) c.3065G>C (p.Arg1022Pro) n.3115G>C c.3317G>C (p.Arg1106Pro) c.3218G>C (p.Arg1073Pro) c.3632G>C (p.Arg1211Pro) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.9764068C>T | CA7896309 | GRIN2A | c.3476G>A (p.Arg1159His) c.3005G>A (p.Arg1002His) n.3069G>A c.*846G>A (n.*846G>A) c.3065G>A (p.Arg1022His) n.3115G>A c.3317G>A (p.Arg1106His) c.3218G>A (p.Arg1073His) c.3632G>A (p.Arg1211His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
16 | g.9764069G>A | CA394707619 | GRIN2A | c.3475C>T (p.Arg1159Cys) c.3004C>T (p.Arg1002Cys) n.3068C>T c.*845C>T (n.*845C>T) c.3064C>T (p.Arg1022Cys) n.3114C>T c.3316C>T (p.Arg1106Cys) c.3217C>T (p.Arg1073Cys) c.3631C>T (p.Arg1211Cys) | ClinVar dbSNP gnomAD v4 COSMIC |
16 | g.9764069G>C | CA394707615 | GRIN2A | c.3475C>G (p.Arg1159Gly) c.3004C>G (p.Arg1002Gly) n.3068C>G c.*845C>G (n.*845C>G) c.3064C>G (p.Arg1022Gly) n.3114C>G c.3316C>G (p.Arg1106Gly) c.3217C>G (p.Arg1073Gly) c.3631C>G (p.Arg1211Gly) | dbSNP |
16 | g.9764069G= | CA2206693036 | GRIN2A | c.3475C= (p.Arg1159=) c.3004C= (p.Arg1002=) n.3068C= c.*845C= (n.*845C=) c.3064C= (p.Arg1022=) n.3114C= c.3316C= (p.Arg1106=) c.3217C= (p.Arg1073=) c.3631C= (p.Arg1211=) | |
16 | g.9764069G>T | CA394707617 | GRIN2A | c.3475C>A (p.Arg1159Ser) c.3004C>A (p.Arg1002Ser) n.3068C>A c.*845C>A (n.*845C>A) c.3064C>A (p.Arg1022Ser) n.3114C>A c.3316C>A (p.Arg1106Ser) c.3217C>A (p.Arg1073Ser) c.3631C>A (p.Arg1211Ser) | |
16 | g.9764070dup | CA2580611806 | GRIN2A | c.3475dup (p.Arg1159ProfsTer16) c.3004dup (p.Arg1002ProfsTer16) n.3068dup c.*845dup (n.*845dup) c.3064dup (p.Arg1022ProfsTer16) n.3114dup c.3316dup (p.Arg1106ProfsTer16) c.3217dup (p.Arg1073ProfsTer16) c.3631dup (p.Arg1211ProfsTer16) | |
16 | g.9764070G>A | CA493693428 | GRIN2A | c.3474C>T (p.Phe1158=) c.3003C>T (p.Phe1001=) n.3067C>T c.*844C>T (n.*844C>T) c.3063C>T (p.Phe1021=) n.3113C>T c.3315C>T (p.Phe1105=) c.3216C>T (p.Phe1072=) c.3630C>T (p.Phe1210=) | dbSNP COSMIC |
16 | g.9764070G>C | CA394707622 | GRIN2A | c.3474C>G (p.Phe1158Leu) c.3003C>G (p.Phe1001Leu) n.3067C>G c.*844C>G (n.*844C>G) c.3063C>G (p.Phe1021Leu) n.3113C>G c.3315C>G (p.Phe1105Leu) c.3216C>G (p.Phe1072Leu) c.3630C>G (p.Phe1210Leu) | dbSNP |
16 | g.9764070G>T | CA394707624 | GRIN2A | c.3474C>A (p.Phe1158Leu) c.3003C>A (p.Phe1001Leu) n.3067C>A c.*844C>A (n.*844C>A) c.3063C>A (p.Phe1021Leu) n.3113C>A c.3315C>A (p.Phe1105Leu) c.3216C>A (p.Phe1072Leu) c.3630C>A (p.Phe1210Leu) | COSMIC |
16 | g.9764071A>C | CA394707626 | GRIN2A | c.3473T>G (p.Phe1158Cys) c.3002T>G (p.Phe1001Cys) n.3066T>G c.*843T>G (n.*843T>G) c.3062T>G (p.Phe1021Cys) n.3112T>G c.3314T>G (p.Phe1105Cys) c.3215T>G (p.Phe1072Cys) c.3629T>G (p.Phe1210Cys) | gnomAD v4 |
16 | g.9764071A>G | CA394707628 | GRIN2A | c.3473T>C (p.Phe1158Ser) c.3002T>C (p.Phe1001Ser) n.3066T>C c.*843T>C (n.*843T>C) c.3062T>C (p.Phe1021Ser) n.3112T>C c.3314T>C (p.Phe1105Ser) c.3215T>C (p.Phe1072Ser) c.3629T>C (p.Phe1210Ser) | dbSNP |
16 | g.9764071A>T | CA394707630 | GRIN2A | c.3473T>A (p.Phe1158Tyr) c.3002T>A (p.Phe1001Tyr) n.3066T>A c.*843T>A (n.*843T>A) c.3062T>A (p.Phe1021Tyr) n.3112T>A c.3314T>A (p.Phe1105Tyr) c.3215T>A (p.Phe1072Tyr) c.3629T>A (p.Phe1210Tyr) | |
16 | g.9764072A>C | CA394707631 | GRIN2A | c.3472T>G (p.Phe1158Val) c.3001T>G (p.Phe1001Val) n.3065T>G c.*842T>G (n.*842T>G) c.3061T>G (p.Phe1021Val) n.3111T>G c.3313T>G (p.Phe1105Val) c.3214T>G (p.Phe1072Val) c.3628T>G (p.Phe1210Val) | |
16 | g.9764072A>G | CA394707633 | GRIN2A | c.3472T>C (p.Phe1158Leu) c.3001T>C (p.Phe1001Leu) n.3065T>C c.*842T>C (n.*842T>C) c.3061T>C (p.Phe1021Leu) n.3111T>C c.3313T>C (p.Phe1105Leu) c.3214T>C (p.Phe1072Leu) c.3628T>C (p.Phe1210Leu) | |
16 | g.9764072A>T | CA394707635 | GRIN2A | c.3472T>A (p.Phe1158Ile) c.3001T>A (p.Phe1001Ile) n.3065T>A c.*842T>A (n.*842T>A) c.3061T>A (p.Phe1021Ile) n.3111T>A c.3313T>A (p.Phe1105Ile) c.3214T>A (p.Phe1072Ile) c.3628T>A (p.Phe1210Ile) | dbSNP |
16 | g.9764073G>A | CA277537250 | GRIN2A | c.3471C>T (p.Asn1157=) c.3000C>T (p.Asn1000=) n.3064C>T c.*841C>T (n.*841C>T) c.3060C>T (p.Asn1020=) n.3110C>T c.3312C>T (p.Asn1104=) c.3213C>T (p.Asn1071=) c.3627C>T (p.Asn1209=) | dbSNP |
16 | g.9764073G>C | CA394707639 | GRIN2A | c.3471C>G (p.Asn1157Lys) c.3000C>G (p.Asn1000Lys) n.3064C>G c.*841C>G (n.*841C>G) c.3060C>G (p.Asn1020Lys) n.3110C>G c.3312C>G (p.Asn1104Lys) c.3213C>G (p.Asn1071Lys) c.3627C>G (p.Asn1209Lys) | dbSNP |
16 | g.9764073G= | CA2206693037 | GRIN2A | c.3471C= (p.Asn1157=) c.3000C= (p.Asn1000=) n.3064C= c.*841C= (n.*841C=) c.3060C= (p.Asn1020=) n.3110C= c.3312C= (p.Asn1104=) c.3213C= (p.Asn1071=) c.3627C= (p.Asn1209=) | |
16 | g.9764073G>T | CA7896312 | GRIN2A | c.3471C>A (p.Asn1157Lys) c.3000C>A (p.Asn1000Lys) n.3064C>A c.*841C>A (n.*841C>A) c.3060C>A (p.Asn1020Lys) n.3110C>A c.3312C>A (p.Asn1104Lys) c.3213C>A (p.Asn1071Lys) c.3627C>A (p.Asn1209Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.9764074T>A | CA394707644 | GRIN2A | c.3470A>T (p.Asn1157Ile) c.2999A>T (p.Asn1000Ile) n.3063A>T c.*840A>T (n.*840A>T) c.3059A>T (p.Asn1020Ile) n.3109A>T c.3311A>T (p.Asn1104Ile) c.3212A>T (p.Asn1071Ile) c.3626A>T (p.Asn1209Ile) | dbSNP |
16 | g.9764074T>C | CA394707647 | GRIN2A | c.3470A>G (p.Asn1157Ser) c.2999A>G (p.Asn1000Ser) n.3063A>G c.*840A>G (n.*840A>G) c.3059A>G (p.Asn1020Ser) n.3109A>G c.3311A>G (p.Asn1104Ser) c.3212A>G (p.Asn1071Ser) c.3626A>G (p.Asn1209Ser) | |
16 | g.9764074T>G | CA394707643 | GRIN2A | c.3470A>C (p.Asn1157Thr) c.2999A>C (p.Asn1000Thr) n.3063A>C c.*840A>C (n.*840A>C) c.3059A>C (p.Asn1020Thr) n.3109A>C c.3311A>C (p.Asn1104Thr) c.3212A>C (p.Asn1071Thr) c.3626A>C (p.Asn1209Thr) | dbSNP |
16 | g.9764075T>A | CA394707653 | GRIN2A | c.3469A>T (p.Asn1157Tyr) c.2998A>T (p.Asn1000Tyr) n.3062A>T c.*839A>T (n.*839A>T) c.3058A>T (p.Asn1020Tyr) n.3108A>T c.3310A>T (p.Asn1104Tyr) c.3211A>T (p.Asn1071Tyr) c.3625A>T (p.Asn1209Tyr) | dbSNP |
16 | g.9764075T>C | CA394707649 | GRIN2A | c.3469A>G (p.Asn1157Asp) c.2998A>G (p.Asn1000Asp) n.3062A>G c.*839A>G (n.*839A>G) c.3058A>G (p.Asn1020Asp) n.3108A>G c.3310A>G (p.Asn1104Asp) c.3211A>G (p.Asn1071Asp) c.3625A>G (p.Asn1209Asp) | |
16 | g.9764075T>G | CA394707652 | GRIN2A | c.3469A>C (p.Asn1157His) c.2998A>C (p.Asn1000His) n.3062A>C c.*839A>C (n.*839A>C) c.3058A>C (p.Asn1020His) n.3108A>C c.3310A>C (p.Asn1104His) c.3211A>C (p.Asn1071His) c.3625A>C (p.Asn1209His) | dbSNP |
16 | g.9764076T>A | CA7896313 | GRIN2A | c.3468A>T (p.Glu1156Asp) c.2997A>T (p.Glu999Asp) n.3061A>T c.*838A>T (n.*838A>T) c.3057A>T (p.Glu1019Asp) n.3107A>T c.3309A>T (p.Glu1103Asp) c.3210A>T (p.Glu1070Asp) c.3624A>T (p.Glu1208Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.9764076T>C | CA493693437 | GRIN2A | c.3468A>G (p.Glu1156=) c.2997A>G (p.Glu999=) n.3061A>G c.*838A>G (n.*838A>G) c.3057A>G (p.Glu1019=) n.3107A>G c.3309A>G (p.Glu1103=) c.3210A>G (p.Glu1070=) c.3624A>G (p.Glu1208=) | dbSNP |
16 | g.9764076T>G | CA394707657 | GRIN2A | c.3468A>C (p.Glu1156Asp) c.2997A>C (p.Glu999Asp) n.3061A>C c.*838A>C (n.*838A>C) c.3057A>C (p.Glu1019Asp) n.3107A>C c.3309A>C (p.Glu1103Asp) c.3210A>C (p.Glu1070Asp) c.3624A>C (p.Glu1208Asp) | |
16 | g.9764076T= | CA2206693038 | GRIN2A | c.3468A= (p.Glu1156=) c.2997A= (p.Glu999=) n.3061A= c.*838A= (n.*838A=) c.3057A= (p.Glu1019=) n.3107A= c.3309A= (p.Glu1103=) c.3210A= (p.Glu1070=) c.3624A= (p.Glu1208=) | |
16 | g.9764077T>A | CA394707659 | GRIN2A | c.3467A>T (p.Glu1156Val) c.2996A>T (p.Glu999Val) n.3060A>T c.*837A>T (n.*837A>T) c.3056A>T (p.Glu1019Val) n.3106A>T c.3308A>T (p.Glu1103Val) c.3209A>T (p.Glu1070Val) c.3623A>T (p.Glu1208Val) | dbSNP |
16 | g.9764077T>C | CA394707661 | GRIN2A | c.3467A>G (p.Glu1156Gly) c.2996A>G (p.Glu999Gly) n.3060A>G c.*837A>G (n.*837A>G) c.3056A>G (p.Glu1019Gly) n.3106A>G c.3308A>G (p.Glu1103Gly) c.3209A>G (p.Glu1070Gly) c.3623A>G (p.Glu1208Gly) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.9764077T>G | CA394707663 | GRIN2A | c.3467A>C (p.Glu1156Ala) c.2996A>C (p.Glu999Ala) n.3060A>C c.*837A>C (n.*837A>C) c.3056A>C (p.Glu1019Ala) n.3106A>C c.3308A>C (p.Glu1103Ala) c.3209A>C (p.Glu1070Ala) c.3623A>C (p.Glu1208Ala) | |
16 | g.9764077T= | CA2206693039 | GRIN2A | c.3467A= (p.Glu1156=) c.2996A= (p.Glu999=) n.3060A= c.*837A= (n.*837A=) c.3056A= (p.Glu1019=) n.3106A= c.3308A= (p.Glu1103=) c.3209A= (p.Glu1070=) c.3623A= (p.Glu1208=) | |
16 | g.9764078C>A | CA394707666 | GRIN2A | c.3466G>T (p.Glu1156Ter) c.2995G>T (p.Glu999Ter) n.3059G>T c.*836G>T (n.*836G>T) c.3055G>T (p.Glu1019Ter) n.3105G>T c.3307G>T (p.Glu1103Ter) c.3208G>T (p.Glu1070Ter) c.3622G>T (p.Glu1208Ter) | dbSNP |
16 | g.9764078C= | CA2206693040 | GRIN2A | c.3466G= (p.Glu1156=) c.2995G= (p.Glu999=) n.3059G= c.*836G= (n.*836G=) c.3055G= (p.Glu1019=) n.3105G= c.3307G= (p.Glu1103=) c.3208G= (p.Glu1070=) c.3622G= (p.Glu1208=) | |
16 | g.9764078C>G | CA394707668 | GRIN2A | c.3466G>C (p.Glu1156Gln) c.2995G>C (p.Glu999Gln) n.3059G>C c.*836G>C (n.*836G>C) c.3055G>C (p.Glu1019Gln) n.3105G>C c.3307G>C (p.Glu1103Gln) c.3208G>C (p.Glu1070Gln) c.3622G>C (p.Glu1208Gln) | dbSNP |
16 | g.9764078C>T | CA394707669 | GRIN2A | c.3466G>A (p.Glu1156Lys) c.2995G>A (p.Glu999Lys) n.3059G>A c.*836G>A (n.*836G>A) c.3055G>A (p.Glu1019Lys) n.3105G>A c.3307G>A (p.Glu1103Lys) c.3208G>A (p.Glu1070Lys) c.3622G>A (p.Glu1208Lys) | dbSNP gnomAD v4 COSMIC |
16 | g.9764079A>C | CA394707672 | GRIN2A | c.3465T>G (p.Ser1155Arg) c.2994T>G (p.Ser998Arg) n.3058T>G c.*835T>G (n.*835T>G) c.3054T>G (p.Ser1018Arg) n.3104T>G c.3306T>G (p.Ser1102Arg) c.3207T>G (p.Ser1069Arg) c.3621T>G (p.Ser1207Arg) | ClinVar dbSNP |
16 | g.9764079A>G | CA493693442 | GRIN2A | c.3465T>C (p.Ser1155=) c.2994T>C (p.Ser998=) n.3058T>C c.*835T>C (n.*835T>C) c.3054T>C (p.Ser1018=) n.3104T>C c.3306T>C (p.Ser1102=) c.3207T>C (p.Ser1069=) c.3621T>C (p.Ser1207=) | |
16 | g.9764079A>T | CA394707674 | GRIN2A | c.3465T>A (p.Ser1155Arg) c.2994T>A (p.Ser998Arg) n.3058T>A c.*835T>A (n.*835T>A) c.3054T>A (p.Ser1018Arg) n.3104T>A c.3306T>A (p.Ser1102Arg) c.3207T>A (p.Ser1069Arg) c.3621T>A (p.Ser1207Arg) | dbSNP |
16 | g.9764080C>A | CA7896314 | GRIN2A | c.3464G>T (p.Ser1155Ile) c.2993G>T (p.Ser998Ile) n.3057G>T c.*834G>T (n.*834G>T) c.3053G>T (p.Ser1018Ile) n.3103G>T c.3305G>T (p.Ser1102Ile) c.3206G>T (p.Ser1069Ile) c.3620G>T (p.Ser1207Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.9764080C= | CA2206693041 | GRIN2A | c.3464G= (p.Ser1155=) c.2993G= (p.Ser998=) n.3057G= c.*834G= (n.*834G=) c.3053G= (p.Ser1018=) n.3103G= c.3305G= (p.Ser1102=) c.3206G= (p.Ser1069=) c.3620G= (p.Ser1207=) | |
16 | g.9764080C>G | CA394707678 | GRIN2A | c.3464G>C (p.Ser1155Thr) c.2993G>C (p.Ser998Thr) n.3057G>C c.*834G>C (n.*834G>C) c.3053G>C (p.Ser1018Thr) n.3103G>C c.3305G>C (p.Ser1102Thr) c.3206G>C (p.Ser1069Thr) c.3620G>C (p.Ser1207Thr) | dbSNP |
16 | g.9764080C>T | CA394707679 | GRIN2A | c.3464G>A (p.Ser1155Asn) c.2993G>A (p.Ser998Asn) n.3057G>A c.*834G>A (n.*834G>A) c.3053G>A (p.Ser1018Asn) n.3103G>A c.3305G>A (p.Ser1102Asn) c.3206G>A (p.Ser1069Asn) c.3620G>A (p.Ser1207Asn) | dbSNP |
16 | g.9764081T>A | CA394707682 | GRIN2A | c.3463A>T (p.Ser1155Cys) c.2992A>T (p.Ser998Cys) n.3056A>T c.*833A>T (n.*833A>T) c.3052A>T (p.Ser1018Cys) n.3102A>T c.3304A>T (p.Ser1102Cys) c.3205A>T (p.Ser1069Cys) c.3619A>T (p.Ser1207Cys) | |
16 | g.9764081T>C | CA394707684 | GRIN2A | c.3463A>G (p.Ser1155Gly) c.2992A>G (p.Ser998Gly) n.3056A>G c.*833A>G (n.*833A>G) c.3052A>G (p.Ser1018Gly) n.3102A>G c.3304A>G (p.Ser1102Gly) c.3205A>G (p.Ser1069Gly) c.3619A>G (p.Ser1207Gly) | |
16 | g.9764081T>G | CA394707686 | GRIN2A | c.3463A>C (p.Ser1155Arg) c.2992A>C (p.Ser998Arg) n.3056A>C c.*833A>C (n.*833A>C) c.3052A>C (p.Ser1018Arg) n.3102A>C c.3304A>C (p.Ser1102Arg) c.3205A>C (p.Ser1069Arg) c.3619A>C (p.Ser1207Arg) | |
16 | g.9764082G>A | CA493693447 | GRIN2A | c.3462C>T (p.Pro1154=) c.2991C>T (p.Pro997=) n.3055C>T c.*832C>T (n.*832C>T) c.3051C>T (p.Pro1017=) n.3101C>T c.3303C>T (p.Pro1101=) c.3204C>T (p.Pro1068=) c.3618C>T (p.Pro1206=) | dbSNP |
16 | g.9764082G>C | CA493693448 | GRIN2A | c.3462C>G (p.Pro1154=) c.2991C>G (p.Pro997=) n.3055C>G c.*832C>G (n.*832C>G) c.3051C>G (p.Pro1017=) n.3101C>G c.3303C>G (p.Pro1101=) c.3204C>G (p.Pro1068=) c.3618C>G (p.Pro1206=) | |
16 | g.9764082G>T | CA493693449 | GRIN2A | c.3462C>A (p.Pro1154=) c.2991C>A (p.Pro997=) n.3055C>A c.*832C>A (n.*832C>A) c.3051C>A (p.Pro1017=) n.3101C>A c.3303C>A (p.Pro1101=) c.3204C>A (p.Pro1068=) c.3618C>A (p.Pro1206=) | dbSNP |
16 | g.9764083G>A | CA394707689 | GRIN2A | c.3461C>T (p.Pro1154Leu) c.2990C>T (p.Pro997Leu) n.3054C>T c.*831C>T (n.*831C>T) c.3050C>T (p.Pro1017Leu) n.3100C>T c.3302C>T (p.Pro1101Leu) c.3203C>T (p.Pro1068Leu) c.3617C>T (p.Pro1206Leu) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.9764083G>C | CA394707691 | GRIN2A | c.3461C>G (p.Pro1154Arg) c.2990C>G (p.Pro997Arg) n.3054C>G c.*831C>G (n.*831C>G) c.3050C>G (p.Pro1017Arg) n.3100C>G c.3302C>G (p.Pro1101Arg) c.3203C>G (p.Pro1068Arg) c.3617C>G (p.Pro1206Arg) | dbSNP |
16 | g.9764083G= | CA2206693042 | GRIN2A | c.3461C= (p.Pro1154=) c.2990C= (p.Pro997=) n.3054C= c.*831C= (n.*831C=) c.3050C= (p.Pro1017=) n.3100C= c.3302C= (p.Pro1101=) c.3203C= (p.Pro1068=) c.3617C= (p.Pro1206=) | |
16 | g.9764083G>T | CA394707693 | GRIN2A | c.3461C>A (p.Pro1154His) c.2990C>A (p.Pro997His) n.3054C>A c.*831C>A (n.*831C>A) c.3050C>A (p.Pro1017His) n.3100C>A c.3302C>A (p.Pro1101His) c.3203C>A (p.Pro1068His) c.3617C>A (p.Pro1206His) | dbSNP |
16 | g.9764084G>A | CA394707696 | GRIN2A | c.3460C>T (p.Pro1154Ser) c.2989C>T (p.Pro997Ser) n.3053C>T c.*830C>T (n.*830C>T) c.3049C>T (p.Pro1017Ser) n.3099C>T c.3301C>T (p.Pro1101Ser) c.3202C>T (p.Pro1068Ser) c.3616C>T (p.Pro1206Ser) | dbSNP gnomAD v4 |
16 | g.9764084G>C | CA394707697 | GRIN2A | c.3460C>G (p.Pro1154Ala) c.2989C>G (p.Pro997Ala) n.3053C>G c.*830C>G (n.*830C>G) c.3049C>G (p.Pro1017Ala) n.3099C>G c.3301C>G (p.Pro1101Ala) c.3202C>G (p.Pro1068Ala) c.3616C>G (p.Pro1206Ala) | dbSNP |
16 | g.9764084G= | CA2206693043 | GRIN2A | c.3460C= (p.Pro1154=) c.2989C= (p.Pro997=) n.3053C= c.*830C= (n.*830C=) c.3049C= (p.Pro1017=) n.3099C= c.3301C= (p.Pro1101=) c.3202C= (p.Pro1068=) c.3616C= (p.Pro1206=) | |
16 | g.9764084G>T | CA394707699 | GRIN2A | c.3460C>A (p.Pro1154Thr) c.2989C>A (p.Pro997Thr) n.3053C>A c.*830C>A (n.*830C>A) c.3049C>A (p.Pro1017Thr) n.3099C>A c.3301C>A (p.Pro1101Thr) c.3202C>A (p.Pro1068Thr) c.3616C>A (p.Pro1206Thr) | ClinVar dbSNP gnomAD v4 |
16 | g.9764085A>C | CA394707702 | GRIN2A | c.3459T>G (p.Asp1153Glu) c.2988T>G (p.Asp996Glu) n.3052T>G c.*829T>G (n.*829T>G) c.3048T>G (p.Asp1016Glu) n.3098T>G c.3300T>G (p.Asp1100Glu) c.3201T>G (p.Asp1067Glu) c.3615T>G (p.Asp1205Glu) | |
16 | g.9764085A>G | CA493693456 | GRIN2A | c.3459T>C (p.Asp1153=) c.2988T>C (p.Asp996=) n.3052T>C c.*829T>C (n.*829T>C) c.3048T>C (p.Asp1016=) n.3098T>C c.3300T>C (p.Asp1100=) c.3201T>C (p.Asp1067=) c.3615T>C (p.Asp1205=) | dbSNP |
16 | g.9764085A>T | CA394707703 | GRIN2A | c.3459T>A (p.Asp1153Glu) c.2988T>A (p.Asp996Glu) n.3052T>A c.*829T>A (n.*829T>A) c.3048T>A (p.Asp1016Glu) n.3098T>A c.3300T>A (p.Asp1100Glu) c.3201T>A (p.Asp1067Glu) c.3615T>A (p.Asp1205Glu) | dbSNP |
16 | g.9764086T>A | CA394707709 | GRIN2A | c.3458A>T (p.Asp1153Val) c.2987A>T (p.Asp996Val) n.3051A>T c.*828A>T (n.*828A>T) c.3047A>T (p.Asp1016Val) n.3097A>T c.3299A>T (p.Asp1100Val) c.3200A>T (p.Asp1067Val) c.3614A>T (p.Asp1205Val) | dbSNP |
16 | g.9764086T>C | CA394707711 | GRIN2A | c.3458A>G (p.Asp1153Gly) c.2987A>G (p.Asp996Gly) n.3051A>G c.*828A>G (n.*828A>G) c.3047A>G (p.Asp1016Gly) n.3097A>G c.3299A>G (p.Asp1100Gly) c.3200A>G (p.Asp1067Gly) c.3614A>G (p.Asp1205Gly) | |
16 | g.9764086T>G | CA394707707 | GRIN2A | c.3458A>C (p.Asp1153Ala) c.2987A>C (p.Asp996Ala) n.3051A>C c.*828A>C (n.*828A>C) c.3047A>C (p.Asp1016Ala) n.3097A>C c.3299A>C (p.Asp1100Ala) c.3200A>C (p.Asp1067Ala) c.3614A>C (p.Asp1205Ala) | dbSNP |
16 | g.9764087C>A | CA394707714 | GRIN2A | c.3457G>T (p.Asp1153Tyr) c.2986G>T (p.Asp996Tyr) n.3050G>T c.*827G>T (n.*827G>T) c.3046G>T (p.Asp1016Tyr) n.3096G>T c.3298G>T (p.Asp1100Tyr) c.3199G>T (p.Asp1067Tyr) c.3613G>T (p.Asp1205Tyr) | ClinVar dbSNP |
16 | g.9764087C= | CA2206693044 | GRIN2A | c.3457G= (p.Asp1153=) c.2986G= (p.Asp996=) n.3050G= c.*827G= (n.*827G=) c.3046G= (p.Asp1016=) n.3096G= c.3298G= (p.Asp1100=) c.3199G= (p.Asp1067=) c.3613G= (p.Asp1205=) | |
16 | g.9764087C>G | CA394707716 | GRIN2A | c.3457G>C (p.Asp1153His) c.2986G>C (p.Asp996His) n.3050G>C c.*827G>C (n.*827G>C) c.3046G>C (p.Asp1016His) n.3096G>C c.3298G>C (p.Asp1100His) c.3199G>C (p.Asp1067His) c.3613G>C (p.Asp1205His) | dbSNP |
16 | g.9764087C>T | CA277537260 | GRIN2A | c.3457G>A (p.Asp1153Asn) c.2986G>A (p.Asp996Asn) n.3050G>A c.*827G>A (n.*827G>A) c.3046G>A (p.Asp1016Asn) n.3096G>A c.3298G>A (p.Asp1100Asn) c.3199G>A (p.Asp1067Asn) c.3613G>A (p.Asp1205Asn) | dbSNP COSMIC |
16 | g.9764088C>A | CA394707719 | GRIN2A | c.3456G>T (p.Gln1152His) c.2985G>T (p.Gln995His) n.3049G>T c.*826G>T (n.*826G>T) c.3045G>T (p.Gln1015His) n.3095G>T c.3297G>T (p.Gln1099His) c.3198G>T (p.Gln1066His) c.3612G>T (p.Gln1204His) | dbSNP |
16 | g.9764088C= | CA2206693045 | GRIN2A | c.3456G= (p.Gln1152=) c.2985G= (p.Gln995=) n.3049G= c.*826G= (n.*826G=) c.3045G= (p.Gln1015=) n.3095G= c.3297G= (p.Gln1099=) c.3198G= (p.Gln1066=) c.3612G= (p.Gln1204=) | |
16 | g.9764088C>G | CA394707721 | GRIN2A | c.3456G>C (p.Gln1152His) c.2985G>C (p.Gln995His) n.3049G>C c.*826G>C (n.*826G>C) c.3045G>C (p.Gln1015His) n.3095G>C c.3297G>C (p.Gln1099His) c.3198G>C (p.Gln1066His) c.3612G>C (p.Gln1204His) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
16 | g.9764088C>T | CA493693459 | GRIN2A | c.3456G>A (p.Gln1152=) c.2985G>A (p.Gln995=) n.3049G>A c.*826G>A (n.*826G>A) c.3045G>A (p.Gln1015=) n.3095G>A c.3297G>A (p.Gln1099=) c.3198G>A (p.Gln1066=) c.3612G>A (p.Gln1204=) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
16 | g.9764089T>A | CA394707724 | GRIN2A | c.3455A>T (p.Gln1152Leu) c.2984A>T (p.Gln995Leu) n.3048A>T c.*825A>T (n.*825A>T) c.3044A>T (p.Gln1015Leu) n.3094A>T c.3296A>T (p.Gln1099Leu) c.3197A>T (p.Gln1066Leu) c.3611A>T (p.Gln1204Leu) | gnomAD v4 |
16 | g.9764089T>C | CA394707726 | GRIN2A | c.3455A>G (p.Gln1152Arg) c.2984A>G (p.Gln995Arg) n.3048A>G c.*825A>G (n.*825A>G) c.3044A>G (p.Gln1015Arg) n.3094A>G c.3296A>G (p.Gln1099Arg) c.3197A>G (p.Gln1066Arg) c.3611A>G (p.Gln1204Arg) | |
16 | g.9764089T>G | CA394707728 | GRIN2A | c.3455A>C (p.Gln1152Pro) c.2984A>C (p.Gln995Pro) n.3048A>C c.*825A>C (n.*825A>C) c.3044A>C (p.Gln1015Pro) n.3094A>C c.3296A>C (p.Gln1099Pro) c.3197A>C (p.Gln1066Pro) c.3611A>C (p.Gln1204Pro) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.9764089T= | CA2206693046 | GRIN2A | c.3455A= (p.Gln1152=) c.2984A= (p.Gln995=) n.3048A= c.*825A= (n.*825A=) c.3044A= (p.Gln1015=) n.3094A= c.3296A= (p.Gln1099=) c.3197A= (p.Gln1066=) c.3611A= (p.Gln1204=) | |
16 | g.9764090G>A | CA394707730 | GRIN2A | c.3454C>T (p.Gln1152Ter) c.2983C>T (p.Gln995Ter) n.3047C>T c.*824C>T (n.*824C>T) c.3043C>T (p.Gln1015Ter) n.3093C>T c.3295C>T (p.Gln1099Ter) c.3196C>T (p.Gln1066Ter) c.3610C>T (p.Gln1204Ter) | dbSNP |
16 | g.9764090G>C | CA394707732 | GRIN2A | c.3454C>G (p.Gln1152Glu) c.2983C>G (p.Gln995Glu) n.3047C>G c.*824C>G (n.*824C>G) c.3043C>G (p.Gln1015Glu) n.3093C>G c.3295C>G (p.Gln1099Glu) c.3196C>G (p.Gln1066Glu) c.3610C>G (p.Gln1204Glu) | dbSNP gnomAD v4 |
16 | g.9764090G= | CA2206693047 | GRIN2A | c.3454C= (p.Gln1152=) c.2983C= (p.Gln995=) n.3047C= c.*824C= (n.*824C=) c.3043C= (p.Gln1015=) n.3093C= c.3295C= (p.Gln1099=) c.3196C= (p.Gln1066=) c.3610C= (p.Gln1204=) | |
16 | g.9764090G>T | CA394707733 | GRIN2A | c.3454C>A (p.Gln1152Lys) c.2983C>A (p.Gln995Lys) n.3047C>A c.*824C>A (n.*824C>A) c.3043C>A (p.Gln1015Lys) n.3093C>A c.3295C>A (p.Gln1099Lys) c.3196C>A (p.Gln1066Lys) c.3610C>A (p.Gln1204Lys) | dbSNP |
16 | g.9764091G>A | CA493693463 | GRIN2A | c.3453C>T (p.Tyr1151=) c.2982C>T (p.Tyr994=) n.3046C>T c.*823C>T (n.*823C>T) c.3042C>T (p.Tyr1014=) n.3092C>T c.3294C>T (p.Tyr1098=) c.3195C>T (p.Tyr1065=) c.3609C>T (p.Tyr1203=) | gnomAD v4 |
16 | g.9764091G>C | CA394707735 | GRIN2A | c.3453C>G (p.Tyr1151Ter) c.2982C>G (p.Tyr994Ter) n.3046C>G c.*823C>G (n.*823C>G) c.3042C>G (p.Tyr1014Ter) n.3092C>G c.3294C>G (p.Tyr1098Ter) c.3195C>G (p.Tyr1065Ter) c.3609C>G (p.Tyr1203Ter) | dbSNP |
16 | g.9764091G>T | CA394707737 | GRIN2A | c.3453C>A (p.Tyr1151Ter) c.2982C>A (p.Tyr994Ter) n.3046C>A c.*823C>A (n.*823C>A) c.3042C>A (p.Tyr1014Ter) n.3092C>A c.3294C>A (p.Tyr1098Ter) c.3195C>A (p.Tyr1065Ter) c.3609C>A (p.Tyr1203Ter) | dbSNP |
16 | g.9764092T>A | CA394707835 | GRIN2A | c.3452A>T (p.Tyr1151Phe) c.2981A>T (p.Tyr994Phe) n.3045A>T c.*822A>T (n.*822A>T) c.3041A>T (p.Tyr1014Phe) n.3091A>T c.3293A>T (p.Tyr1098Phe) c.3194A>T (p.Tyr1065Phe) c.3608A>T (p.Tyr1203Phe) | dbSNP |
16 | g.9764092T>C | CA394707834 | GRIN2A | c.3452A>G (p.Tyr1151Cys) c.2981A>G (p.Tyr994Cys) n.3045A>G c.*822A>G (n.*822A>G) c.3041A>G (p.Tyr1014Cys) n.3091A>G c.3293A>G (p.Tyr1098Cys) c.3194A>G (p.Tyr1065Cys) c.3608A>G (p.Tyr1203Cys) | dbSNP COSMIC |
16 | g.9764092T>G | CA394707833 | GRIN2A | c.3452A>C (p.Tyr1151Ser) c.2981A>C (p.Tyr994Ser) n.3045A>C c.*822A>C (n.*822A>C) c.3041A>C (p.Tyr1014Ser) n.3091A>C c.3293A>C (p.Tyr1098Ser) c.3194A>C (p.Tyr1065Ser) c.3608A>C (p.Tyr1203Ser) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.9764092T= | CA2206693048 | GRIN2A | c.3452A= (p.Tyr1151=) c.2981A= (p.Tyr994=) n.3045A= c.*822A= (n.*822A=) c.3041A= (p.Tyr1014=) n.3091A= c.3293A= (p.Tyr1098=) c.3194A= (p.Tyr1065=) c.3608A= (p.Tyr1203=) | |
16 | g.9764093A= | CA2206693049 | GRIN2A | c.3451T= (p.Tyr1151=) c.2980T= (p.Tyr994=) n.3044T= c.*821T= (n.*821T=) c.3040T= (p.Tyr1014=) n.3090T= c.3292T= (p.Tyr1098=) c.3193T= (p.Tyr1065=) c.3607T= (p.Tyr1203=) | |
16 | g.9764093A>C | CA394707836 | GRIN2A | c.3451T>G (p.Tyr1151Asp) c.2980T>G (p.Tyr994Asp) n.3044T>G c.*821T>G (n.*821T>G) c.3040T>G (p.Tyr1014Asp) n.3090T>G c.3292T>G (p.Tyr1098Asp) c.3193T>G (p.Tyr1065Asp) c.3607T>G (p.Tyr1203Asp) | |
16 | g.9764093A>G | CA394707837 | GRIN2A | c.3451T>C (p.Tyr1151His) c.2980T>C (p.Tyr994His) n.3044T>C c.*821T>C (n.*821T>C) c.3040T>C (p.Tyr1014His) n.3090T>C c.3292T>C (p.Tyr1098His) c.3193T>C (p.Tyr1065His) c.3607T>C (p.Tyr1203His) | ClinVar dbSNP |
16 | g.9764093A>T | CA315023 | GRIN2A | c.3451T>A (p.Tyr1151Asn) c.2980T>A (p.Tyr994Asn) n.3044T>A c.*821T>A (n.*821T>A) c.3040T>A (p.Tyr1014Asn) n.3090T>A c.3292T>A (p.Tyr1098Asn) c.3193T>A (p.Tyr1065Asn) c.3607T>A (p.Tyr1203Asn) | dbSNP |
16 | g.9764094G>A | CA493692829 | GRIN2A | c.3450C>T (p.Pro1150=) c.2979C>T (p.Pro993=) n.3043C>T c.*820C>T (n.*820C>T) c.3039C>T (p.Pro1013=) n.3089C>T c.3291C>T (p.Pro1097=) c.3192C>T (p.Pro1064=) c.3606C>T (p.Pro1202=) | dbSNP |
16 | g.9764094G>C | CA493692830 | GRIN2A | c.3450C>G (p.Pro1150=) c.2979C>G (p.Pro993=) n.3043C>G c.*820C>G (n.*820C>G) c.3039C>G (p.Pro1013=) n.3089C>G c.3291C>G (p.Pro1097=) c.3192C>G (p.Pro1064=) c.3606C>G (p.Pro1202=) | dbSNP |
16 | g.9764094G>T | CA493692831 | GRIN2A | c.3450C>A (p.Pro1150=) c.2979C>A (p.Pro993=) n.3043C>A c.*820C>A (n.*820C>A) c.3039C>A (p.Pro1013=) n.3089C>A c.3291C>A (p.Pro1097=) c.3192C>A (p.Pro1064=) c.3606C>A (p.Pro1202=) | |
16 | g.9764095G>A | CA394707838 | GRIN2A | c.3449C>T (p.Pro1150Leu) c.2978C>T (p.Pro993Leu) n.3042C>T c.*819C>T (n.*819C>T) c.3038C>T (p.Pro1013Leu) n.3088C>T c.3290C>T (p.Pro1097Leu) c.3191C>T (p.Pro1064Leu) c.3605C>T (p.Pro1202Leu) | dbSNP |
16 | g.9764095G>C | CA394707839 | GRIN2A | c.3449C>G (p.Pro1150Arg) c.2978C>G (p.Pro993Arg) n.3042C>G c.*819C>G (n.*819C>G) c.3038C>G (p.Pro1013Arg) n.3088C>G c.3290C>G (p.Pro1097Arg) c.3191C>G (p.Pro1064Arg) c.3605C>G (p.Pro1202Arg) | dbSNP |
16 | g.9764095G>T | CA394707840 | GRIN2A | c.3449C>A (p.Pro1150His) c.2978C>A (p.Pro993His) n.3042C>A c.*819C>A (n.*819C>A) c.3038C>A (p.Pro1013His) n.3088C>A c.3290C>A (p.Pro1097His) c.3191C>A (p.Pro1064His) c.3605C>A (p.Pro1202His) | dbSNP |
16 | g.9764096G>A | CA394707841 | GRIN2A | c.3448C>T (p.Pro1150Ser) c.2977C>T (p.Pro993Ser) n.3041C>T c.*818C>T (n.*818C>T) c.3037C>T (p.Pro1013Ser) n.3087C>T c.3289C>T (p.Pro1097Ser) c.3190C>T (p.Pro1064Ser) c.3604C>T (p.Pro1202Ser) | dbSNP gnomAD v4 |
16 | g.9764096G>C | CA394707842 | GRIN2A | c.3448C>G (p.Pro1150Ala) c.2977C>G (p.Pro993Ala) n.3041C>G c.*818C>G (n.*818C>G) c.3037C>G (p.Pro1013Ala) n.3087C>G c.3289C>G (p.Pro1097Ala) c.3190C>G (p.Pro1064Ala) c.3604C>G (p.Pro1202Ala) | dbSNP |
16 | g.9764096G= | CA2206693050 | GRIN2A | c.3448C= (p.Pro1150=) c.2977C= (p.Pro993=) n.3041C= c.*818C= (n.*818C=) c.3037C= (p.Pro1013=) n.3087C= c.3289C= (p.Pro1097=) c.3190C= (p.Pro1064=) c.3604C= (p.Pro1202=) | |
16 | g.9764096G>T | CA394707843 | GRIN2A | c.3448C>A (p.Pro1150Thr) c.2977C>A (p.Pro993Thr) n.3041C>A c.*818C>A (n.*818C>A) c.3037C>A (p.Pro1013Thr) n.3087C>A c.3289C>A (p.Pro1097Thr) c.3190C>A (p.Pro1064Thr) c.3604C>A (p.Pro1202Thr) | dbSNP |
16 | g.9764097G>A | CA493692832 | GRIN2A | c.3447C>T (p.Asp1149=) c.2976C>T (p.Asp992=) n.3040C>T c.*817C>T (n.*817C>T) c.3036C>T (p.Asp1012=) n.3086C>T c.3288C>T (p.Asp1096=) c.3189C>T (p.Asp1063=) c.3603C>T (p.Asp1201=) | ClinVar dbSNP gnomAD v4 |
16 | g.9764097G>C | CA394707844 | GRIN2A | c.3447C>G (p.Asp1149Glu) c.2976C>G (p.Asp992Glu) n.3040C>G c.*817C>G (n.*817C>G) c.3036C>G (p.Asp1012Glu) n.3086C>G c.3288C>G (p.Asp1096Glu) c.3189C>G (p.Asp1063Glu) c.3603C>G (p.Asp1201Glu) | dbSNP |
16 | g.9764097G>T | CA394707845 | GRIN2A | c.3447C>A (p.Asp1149Glu) c.2976C>A (p.Asp992Glu) n.3040C>A c.*817C>A (n.*817C>A) c.3036C>A (p.Asp1012Glu) n.3086C>A c.3288C>A (p.Asp1096Glu) c.3189C>A (p.Asp1063Glu) c.3603C>A (p.Asp1201Glu) | dbSNP |
16 | g.9764098T>A | CA394707846 | GRIN2A | c.3446A>T (p.Asp1149Val) c.2975A>T (p.Asp992Val) n.3039A>T c.*816A>T (n.*816A>T) c.3035A>T (p.Asp1012Val) n.3085A>T c.3287A>T (p.Asp1096Val) c.3188A>T (p.Asp1063Val) c.3602A>T (p.Asp1201Val) | ClinVar dbSNP |
16 | g.9764098T>C | CA394707847 | GRIN2A | c.3446A>G (p.Asp1149Gly) c.2975A>G (p.Asp992Gly) n.3039A>G c.*816A>G (n.*816A>G) c.3035A>G (p.Asp1012Gly) n.3085A>G c.3287A>G (p.Asp1096Gly) c.3188A>G (p.Asp1063Gly) c.3602A>G (p.Asp1201Gly) | dbSNP |
16 | g.9764098T>G | CA394707848 | GRIN2A | c.3446A>C (p.Asp1149Ala) c.2975A>C (p.Asp992Ala) n.3039A>C c.*816A>C (n.*816A>C) c.3035A>C (p.Asp1012Ala) n.3085A>C c.3287A>C (p.Asp1096Ala) c.3188A>C (p.Asp1063Ala) c.3602A>C (p.Asp1201Ala) | dbSNP |
16 | g.9764099C>A | CA394707850 | GRIN2A | c.3445G>T (p.Asp1149Tyr) c.2974G>T (p.Asp992Tyr) n.3038G>T c.*815G>T (n.*815G>T) c.3034G>T (p.Asp1012Tyr) n.3084G>T c.3286G>T (p.Asp1096Tyr) c.3187G>T (p.Asp1063Tyr) c.3601G>T (p.Asp1201Tyr) | dbSNP |
16 | g.9764099C>G | CA394707851 | GRIN2A | c.3445G>C (p.Asp1149His) c.2974G>C (p.Asp992His) n.3038G>C c.*815G>C (n.*815G>C) c.3034G>C (p.Asp1012His) n.3084G>C c.3286G>C (p.Asp1096His) c.3187G>C (p.Asp1063His) c.3601G>C (p.Asp1201His) | dbSNP |
16 | g.9764099C>T | CA394707849 | GRIN2A | c.3445G>A (p.Asp1149Asn) c.2974G>A (p.Asp992Asn) n.3038G>A c.*815G>A (n.*815G>A) c.3034G>A (p.Asp1012Asn) n.3084G>A c.3286G>A (p.Asp1096Asn) c.3187G>A (p.Asp1063Asn) c.3601G>A (p.Asp1201Asn) | dbSNP gnomAD v4 |
16 | g.9764100C>A | CA493692841 | GRIN2A | c.3444G>T (p.Pro1148=) c.2973G>T (p.Pro991=) n.3037G>T c.*814G>T (n.*814G>T) c.3033G>T (p.Pro1011=) n.3083G>T c.3285G>T (p.Pro1095=) c.3186G>T (p.Pro1062=) c.3600G>T (p.Pro1200=) | ClinVar COSMIC |
16 | g.9764100C= | CA2206693051 | GRIN2A | c.3444G= (p.Pro1148=) c.2973G= (p.Pro991=) n.3037G= c.*814G= (n.*814G=) c.3033G= (p.Pro1011=) n.3083G= c.3285G= (p.Pro1095=) c.3186G= (p.Pro1062=) c.3600G= (p.Pro1200=) | |
16 | g.9764100C>G | CA493692836 | GRIN2A | c.3444G>C (p.Pro1148=) c.2973G>C (p.Pro991=) n.3037G>C c.*814G>C (n.*814G>C) c.3033G>C (p.Pro1011=) n.3083G>C c.3285G>C (p.Pro1095=) c.3186G>C (p.Pro1062=) c.3600G>C (p.Pro1200=) | |
16 | g.9764100C>T | CA493692838 | GRIN2A | c.3444G>A (p.Pro1148=) c.2973G>A (p.Pro991=) n.3037G>A c.*814G>A (n.*814G>A) c.3033G>A (p.Pro1011=) n.3083G>A c.3285G>A (p.Pro1095=) c.3186G>A (p.Pro1062=) c.3600G>A (p.Pro1200=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
16 | g.9764101G>A | CA7896315 | GRIN2A | c.3443C>T (p.Pro1148Leu) c.2972C>T (p.Pro991Leu) n.3036C>T c.*813C>T (n.*813C>T) c.3032C>T (p.Pro1011Leu) n.3082C>T c.3284C>T (p.Pro1095Leu) c.3185C>T (p.Pro1062Leu) c.3599C>T (p.Pro1200Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.9764101G>C | CA394707852 | GRIN2A | c.3443C>G (p.Pro1148Arg) c.2972C>G (p.Pro991Arg) n.3036C>G c.*813C>G (n.*813C>G) c.3032C>G (p.Pro1011Arg) n.3082C>G c.3284C>G (p.Pro1095Arg) c.3185C>G (p.Pro1062Arg) c.3599C>G (p.Pro1200Arg) | dbSNP |
16 | g.9764101G= | CA2206693052 | GRIN2A | c.3443C= (p.Pro1148=) c.2972C= (p.Pro991=) n.3036C= c.*813C= (n.*813C=) c.3032C= (p.Pro1011=) n.3082C= c.3284C= (p.Pro1095=) c.3185C= (p.Pro1062=) c.3599C= (p.Pro1200=) | |
16 | g.9764101G>T | CA394707853 | GRIN2A | c.3443C>A (p.Pro1148Gln) c.2972C>A (p.Pro991Gln) n.3036C>A c.*813C>A (n.*813C>A) c.3032C>A (p.Pro1011Gln) n.3082C>A c.3284C>A (p.Pro1095Gln) c.3185C>A (p.Pro1062Gln) c.3599C>A (p.Pro1200Gln) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.9764102G>A | CA394707854 | GRIN2A | c.3442C>T (p.Pro1148Ser) c.2971C>T (p.Pro991Ser) n.3035C>T c.*812C>T (n.*812C>T) c.3031C>T (p.Pro1011Ser) n.3081C>T c.3283C>T (p.Pro1095Ser) c.3184C>T (p.Pro1062Ser) c.3598C>T (p.Pro1200Ser) | dbSNP gnomAD v4 COSMIC |
16 | g.9764102G>C | CA394707855 | GRIN2A | c.3442C>G (p.Pro1148Ala) c.2971C>G (p.Pro991Ala) n.3035C>G c.*812C>G (n.*812C>G) c.3031C>G (p.Pro1011Ala) n.3081C>G c.3283C>G (p.Pro1095Ala) c.3184C>G (p.Pro1062Ala) c.3598C>G (p.Pro1200Ala) | dbSNP |
16 | g.9764102G>T | CA394707856 | GRIN2A | c.3442C>A (p.Pro1148Thr) c.2971C>A (p.Pro991Thr) n.3035C>A c.*812C>A (n.*812C>A) c.3031C>A (p.Pro1011Thr) n.3081C>A c.3283C>A (p.Pro1095Thr) c.3184C>A (p.Pro1062Thr) c.3598C>A (p.Pro1200Thr) | dbSNP |
16 | g.9764103G>A | CA493692845 | GRIN2A | c.3441C>T (p.Phe1147=) c.2970C>T (p.Phe990=) n.3034C>T c.*811C>T (n.*811C>T) c.3030C>T (p.Phe1010=) n.3080C>T c.3282C>T (p.Phe1094=) c.3183C>T (p.Phe1061=) c.3597C>T (p.Phe1199=) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
16 | g.9764103G>C | CA394707857 | GRIN2A | c.3441C>G (p.Phe1147Leu) c.2970C>G (p.Phe990Leu) n.3034C>G c.*811C>G (n.*811C>G) c.3030C>G (p.Phe1010Leu) n.3080C>G c.3282C>G (p.Phe1094Leu) c.3183C>G (p.Phe1061Leu) c.3597C>G (p.Phe1199Leu) | dbSNP |
16 | g.9764103G= | CA2206693053 | GRIN2A | c.3441C= (p.Phe1147=) c.2970C= (p.Phe990=) n.3034C= c.*811C= (n.*811C=) c.3030C= (p.Phe1010=) n.3080C= c.3282C= (p.Phe1094=) c.3183C= (p.Phe1061=) c.3597C= (p.Phe1199=) | |
16 | g.9764103G>T | CA394707858 | GRIN2A | c.3441C>A (p.Phe1147Leu) c.2970C>A (p.Phe990Leu) n.3034C>A c.*811C>A (n.*811C>A) c.3030C>A (p.Phe1010Leu) n.3080C>A c.3282C>A (p.Phe1094Leu) c.3183C>A (p.Phe1061Leu) c.3597C>A (p.Phe1199Leu) | dbSNP |
16 | g.9764104A>C | CA394707859 | GRIN2A | c.3440T>G (p.Phe1147Cys) c.2969T>G (p.Phe990Cys) n.3033T>G c.*810T>G (n.*810T>G) c.3029T>G (p.Phe1010Cys) n.3079T>G c.3281T>G (p.Phe1094Cys) c.3182T>G (p.Phe1061Cys) c.3596T>G (p.Phe1199Cys) | |
16 | g.9764104A>G | CA394707860 | GRIN2A | c.3440T>C (p.Phe1147Ser) c.2969T>C (p.Phe990Ser) n.3033T>C c.*810T>C (n.*810T>C) c.3029T>C (p.Phe1010Ser) n.3079T>C c.3281T>C (p.Phe1094Ser) c.3182T>C (p.Phe1061Ser) c.3596T>C (p.Phe1199Ser) | dbSNP |
16 | g.9764104A>T | CA394707861 | GRIN2A | c.3440T>A (p.Phe1147Tyr) c.2969T>A (p.Phe990Tyr) n.3033T>A c.*810T>A (n.*810T>A) c.3029T>A (p.Phe1010Tyr) n.3079T>A c.3281T>A (p.Phe1094Tyr) c.3182T>A (p.Phe1061Tyr) c.3596T>A (p.Phe1199Tyr) | dbSNP |
16 | g.9764105A>C | CA394707862 | GRIN2A | c.3439T>G (p.Phe1147Val) c.2968T>G (p.Phe990Val) n.3032T>G c.*809T>G (n.*809T>G) c.3028T>G (p.Phe1010Val) n.3078T>G c.3280T>G (p.Phe1094Val) c.3181T>G (p.Phe1061Val) c.3595T>G (p.Phe1199Val) | |
16 | g.9764105A>G | CA394707863 | GRIN2A | c.3439T>C (p.Phe1147Leu) c.2968T>C (p.Phe990Leu) n.3032T>C c.*809T>C (n.*809T>C) c.3028T>C (p.Phe1010Leu) n.3078T>C c.3280T>C (p.Phe1094Leu) c.3181T>C (p.Phe1061Leu) c.3595T>C (p.Phe1199Leu) | dbSNP |
16 | g.9764105A>T | CA394707864 | GRIN2A | c.3439T>A (p.Phe1147Ile) c.2968T>A (p.Phe990Ile) n.3032T>A c.*809T>A (n.*809T>A) c.3028T>A (p.Phe1010Ile) n.3078T>A c.3280T>A (p.Phe1094Ile) c.3181T>A (p.Phe1061Ile) c.3595T>A (p.Phe1199Ile) | dbSNP |
16 | g.9764106G>A | CA493692851 | GRIN2A | c.3438C>T (p.Asp1146=) c.2967C>T (p.Asp989=) n.3031C>T c.*808C>T (n.*808C>T) c.3027C>T (p.Asp1009=) n.3077C>T c.3279C>T (p.Asp1093=) c.3180C>T (p.Asp1060=) c.3594C>T (p.Asp1198=) | dbSNP gnomAD v4 |
16 | g.9764106G>C | CA394707866 | GRIN2A | c.3438C>G (p.Asp1146Glu) c.2967C>G (p.Asp989Glu) n.3031C>G c.*808C>G (n.*808C>G) c.3027C>G (p.Asp1009Glu) n.3077C>G c.3279C>G (p.Asp1093Glu) c.3180C>G (p.Asp1060Glu) c.3594C>G (p.Asp1198Glu) | dbSNP |
16 | g.9764106G>T | CA394707865 | GRIN2A | c.3438C>A (p.Asp1146Glu) c.2967C>A (p.Asp989Glu) n.3031C>A c.*808C>A (n.*808C>A) c.3027C>A (p.Asp1009Glu) n.3077C>A c.3279C>A (p.Asp1093Glu) c.3180C>A (p.Asp1060Glu) c.3594C>A (p.Asp1198Glu) | |
16 | g.9764107T>A | CA394707867 | GRIN2A | c.3437A>T (p.Asp1146Val) c.2966A>T (p.Asp989Val) n.3030A>T c.*807A>T (n.*807A>T) c.3026A>T (p.Asp1009Val) n.3076A>T c.3278A>T (p.Asp1093Val) c.3179A>T (p.Asp1060Val) c.3593A>T (p.Asp1198Val) | |
16 | g.9764107T>C | CA394707868 | GRIN2A | c.3437A>G (p.Asp1146Gly) c.2966A>G (p.Asp989Gly) n.3030A>G c.*807A>G (n.*807A>G) c.3026A>G (p.Asp1009Gly) n.3076A>G c.3278A>G (p.Asp1093Gly) c.3179A>G (p.Asp1060Gly) c.3593A>G (p.Asp1198Gly) | |
16 | g.9764107T>G | CA394707869 | GRIN2A | c.3437A>C (p.Asp1146Ala) c.2966A>C (p.Asp989Ala) n.3030A>C c.*807A>C (n.*807A>C) c.3026A>C (p.Asp1009Ala) n.3076A>C c.3278A>C (p.Asp1093Ala) c.3179A>C (p.Asp1060Ala) c.3593A>C (p.Asp1198Ala) | |
16 | g.9764108C>A | CA394707870 | GRIN2A | c.3436G>T (p.Asp1146Tyr) c.2965G>T (p.Asp989Tyr) n.3029G>T c.*806G>T (n.*806G>T) c.3025G>T (p.Asp1009Tyr) n.3075G>T c.3277G>T (p.Asp1093Tyr) c.3178G>T (p.Asp1060Tyr) c.3592G>T (p.Asp1198Tyr) | dbSNP |
16 | g.9764108C>G | CA394707871 | GRIN2A | c.3436G>C (p.Asp1146His) c.2965G>C (p.Asp989His) n.3029G>C c.*806G>C (n.*806G>C) c.3025G>C (p.Asp1009His) n.3075G>C c.3277G>C (p.Asp1093His) c.3178G>C (p.Asp1060His) c.3592G>C (p.Asp1198His) | dbSNP |
16 | g.9764108C>T | CA394707872 | GRIN2A | c.3436G>A (p.Asp1146Asn) c.2965G>A (p.Asp989Asn) n.3029G>A c.*806G>A (n.*806G>A) c.3025G>A (p.Asp1009Asn) n.3075G>A c.3277G>A (p.Asp1093Asn) c.3178G>A (p.Asp1060Asn) c.3592G>A (p.Asp1198Asn) | dbSNP |
16 | g.9764109C>A | CA493692854 | GRIN2A | c.3435G>T (p.Val1145=) c.2964G>T (p.Val988=) n.3028G>T c.*805G>T (n.*805G>T) c.3024G>T (p.Val1008=) n.3074G>T c.3276G>T (p.Val1092=) c.3177G>T (p.Val1059=) c.3591G>T (p.Val1197=) | dbSNP |
16 | g.9764109C>G | CA493692855 | GRIN2A | c.3435G>C (p.Val1145=) c.2964G>C (p.Val988=) n.3028G>C c.*805G>C (n.*805G>C) c.3024G>C (p.Val1008=) n.3074G>C c.3276G>C (p.Val1092=) c.3177G>C (p.Val1059=) c.3591G>C (p.Val1197=) | |
16 | g.9764109C>T | CA493692856 | GRIN2A | c.3435G>A (p.Val1145=) c.2964G>A (p.Val988=) n.3028G>A c.*805G>A (n.*805G>A) c.3024G>A (p.Val1008=) n.3074G>A c.3276G>A (p.Val1092=) c.3177G>A (p.Val1059=) c.3591G>A (p.Val1197=) | dbSNP |
16 | g.9764110A>C | CA394707875 | GRIN2A | c.3434T>G (p.Val1145Gly) c.2963T>G (p.Val988Gly) n.3027T>G c.*804T>G (n.*804T>G) c.3023T>G (p.Val1008Gly) n.3073T>G c.3275T>G (p.Val1092Gly) c.3176T>G (p.Val1059Gly) c.3590T>G (p.Val1197Gly) | |
16 | g.9764110A>G | CA394707874 | GRIN2A | c.3434T>C (p.Val1145Ala) c.2963T>C (p.Val988Ala) n.3027T>C c.*804T>C (n.*804T>C) c.3023T>C (p.Val1008Ala) n.3073T>C c.3275T>C (p.Val1092Ala) c.3176T>C (p.Val1059Ala) c.3590T>C (p.Val1197Ala) | dbSNP |
16 | g.9764110A>T | CA394707873 | GRIN2A | c.3434T>A (p.Val1145Glu) c.2963T>A (p.Val988Glu) n.3027T>A c.*804T>A (n.*804T>A) c.3023T>A (p.Val1008Glu) n.3073T>A c.3275T>A (p.Val1092Glu) c.3176T>A (p.Val1059Glu) c.3590T>A (p.Val1197Glu) | dbSNP |
16 | g.9764111C>A | CA394707876 | GRIN2A | c.3433G>T (p.Val1145Leu) c.2962G>T (p.Val988Leu) n.3026G>T c.*803G>T (n.*803G>T) c.3022G>T (p.Val1008Leu) n.3072G>T c.3274G>T (p.Val1092Leu) c.3175G>T (p.Val1059Leu) c.3589G>T (p.Val1197Leu) | dbSNP gnomAD v4 |
16 | g.9764111C= | CA2206693054 | GRIN2A | c.3433G= (p.Val1145=) c.2962G= (p.Val988=) n.3026G= c.*803G= (n.*803G=) c.3022G= (p.Val1008=) n.3072G= c.3274G= (p.Val1092=) c.3175G= (p.Val1059=) c.3589G= (p.Val1197=) | |
16 | g.9764111C>G | CA394707877 | GRIN2A | c.3433G>C (p.Val1145Leu) c.2962G>C (p.Val988Leu) n.3026G>C c.*803G>C (n.*803G>C) c.3022G>C (p.Val1008Leu) n.3072G>C c.3274G>C (p.Val1092Leu) c.3175G>C (p.Val1059Leu) c.3589G>C (p.Val1197Leu) | dbSNP |
16 | g.9764111C>T | CA7896316 | GRIN2A | c.3433G>A (p.Val1145Met) c.2962G>A (p.Val988Met) n.3026G>A c.*803G>A (n.*803G>A) c.3022G>A (p.Val1008Met) n.3072G>A c.3274G>A (p.Val1092Met) c.3175G>A (p.Val1059Met) c.3589G>A (p.Val1197Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
16 | g.9764112G>A | CA7896317 | GRIN2A | c.3432C>T (p.Asn1144=) c.2961C>T (p.Asn987=) n.3025C>T c.*802C>T (n.*802C>T) c.3021C>T (p.Asn1007=) n.3071C>T c.3273C>T (p.Asn1091=) c.3174C>T (p.Asn1058=) c.3588C>T (p.Asn1196=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.9764112G>C | CA394707878 | GRIN2A | c.3432C>G (p.Asn1144Lys) c.2961C>G (p.Asn987Lys) n.3025C>G c.*802C>G (n.*802C>G) c.3021C>G (p.Asn1007Lys) n.3071C>G c.3273C>G (p.Asn1091Lys) c.3174C>G (p.Asn1058Lys) c.3588C>G (p.Asn1196Lys) | dbSNP |
16 | g.9764112G= | CA2206693055 | GRIN2A | c.3432C= (p.Asn1144=) c.2961C= (p.Asn987=) n.3025C= c.*802C= (n.*802C=) c.3021C= (p.Asn1007=) n.3071C= c.3273C= (p.Asn1091=) c.3174C= (p.Asn1058=) c.3588C= (p.Asn1196=) | |
16 | g.9764112G>T | CA394707879 | GRIN2A | c.3432C>A (p.Asn1144Lys) c.2961C>A (p.Asn987Lys) n.3025C>A c.*802C>A (n.*802C>A) c.3021C>A (p.Asn1007Lys) n.3071C>A c.3273C>A (p.Asn1091Lys) c.3174C>A (p.Asn1058Lys) c.3588C>A (p.Asn1196Lys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
16 | g.9764113T>A | CA394707880 | GRIN2A | c.3431A>T (p.Asn1144Ile) c.2960A>T (p.Asn987Ile) n.3024A>T c.*801A>T (n.*801A>T) c.3020A>T (p.Asn1007Ile) n.3070A>T c.3272A>T (p.Asn1091Ile) c.3173A>T (p.Asn1058Ile) c.3587A>T (p.Asn1196Ile) | dbSNP |
16 | g.9764113T>C | CA394707882 | GRIN2A | c.3431A>G (p.Asn1144Ser) c.2960A>G (p.Asn987Ser) n.3024A>G c.*801A>G (n.*801A>G) c.3020A>G (p.Asn1007Ser) n.3070A>G c.3272A>G (p.Asn1091Ser) c.3173A>G (p.Asn1058Ser) c.3587A>G (p.Asn1196Ser) | dbSNP |
16 | g.9764113T>G | CA394707881 | GRIN2A | c.3431A>C (p.Asn1144Thr) c.2960A>C (p.Asn987Thr) n.3024A>C c.*801A>C (n.*801A>C) c.3020A>C (p.Asn1007Thr) n.3070A>C c.3272A>C (p.Asn1091Thr) c.3173A>C (p.Asn1058Thr) c.3587A>C (p.Asn1196Thr) | dbSNP |